Poliklinik für Kieferorthopädie

2022

Einrichtungsstatistik

Forschungsprojekte12
Publikationen9
Vorträge
Promotionen3
Verschiedene wissenschaftliche Aktivitäten

Forschungsprojekte

Projektleiter: Dr. C Erbe, Univ.-Prof. Dr. Dr. H Wehrbein

Staining Potential of two Marketed Fluoride Rinses

Abstract: The objective of this study is to evaluate the stain accumulation potential of two marketed Fluoride rinses in children.
This will be a randomized, parallel group, double-blind, single-center study with two treatment groups comprised of healthy children (10 – 16 years old) with up to 30 subjects per group. A total of up to 60 subjects will participate in this study. At the Baseline visit, subjects will be given an oral exam and a prophylactic cleaning on the twelve anterior teeth. Subjects will be randomly assigned to one of the two treatments. Subjects will then be given a study kit and use it for next two months. Safety and efficacy measurements will be assessed at the Baseline, Week 4 and Week 8 visits.

Laufzeit: 2011-2022
Projektleiter: Dr. C. Erbe, Prof. Dr. Dr. H. Wehrbein

Clinical Study to assess the Plaque removal efficacy of a new manual toothbrush with small brush head

Study Objective
The objective of this study was to evaluate the efficacy of a new Oral-B manual toothbrush (Cross Action small brush head design) verus a control group (Oral-B Indicator 30 soft) in the reduction of dental plaque among a general adult population using the Turesky Modified Quigley-Hein Index (TQHPI).
Product Usage
Acclimation:
Subjects were instructed to brush their teeth at home twice daily (morning and evening) in their customary manner using the assigned provided test toothbrush and their regular toothpaste for approximately one week prior to their on-site visits.
Periods 1-4
Subjects were instructed to brush their teeth as they normally do with the assigned manual brush. The marketed dentifrice was dispensed by site personnel on a tongue depressor. Subjects brushed their teeth without access to a mirror. Brushing time was recorded in a discrete manner by site staff.
Study Design
This was a single-brushing, 2-treatment, examiner-blind, randomized, 4 period, crossover design. Subjects used each of the two toothbrushes twice. 26 adult subjects were enrolled into the clinical trial based on study criteria. For familiarization purposes, subjects were given their assigned test toothbrush to use at home twice daily for approximately one week prior to each study period visit. Subjects were instructed to refrain from all oral hygiene procedures for approximately 24 hours prior to each of their appointment times. In addition, the subjects were instructed to refrain from eating, drinking, chewing gum or smoking (including smokeless tobacco) for 2 hours prior to their appointment time. Only small sips of water were permissible. Subjects were to refrain from sipping water 45 minutes prior to their scheduled visit.
 

Laufzeit: 2018-2023
Projektleiter: Dr. C. Erbe

Histological and histomorphometric investigation of the median palatine suture in different age groups - an ex vivo study on human cadaver specimens

The median palatine suture of the maxilla, which extends from the maxillary incisal fossa to the nasal posterior spine, is of great clinical importance and relevance to orthodontists worldwide. A rapid maxillary expansion (RME) is indicated in the presence of a a narrow upper jaw and / or a one- or bilateral crossbite and / or frontal crowding in order to create space as fast as possible in the transversal.
As the patient ages, the so-called transversal resistance of the median palatine suture becomes larger and thus, it becomes increasingly difficult to predict the success of a conservative RME. Therefore, in patients > 18 years, surgically assisted RME is usually preferred to conservative RME.
Assumptions that the increasing ossification of the suture are responsible for this resistance can only be partially verified. Previous studies showed that at the age of 30 years, only a very small portion of the median suture is clearly ossified, which means that there is still a need for considerable examinations / ex vivo studies.
The aim of this study is to use modern histological and histomorphometric methods to analyze the age-related morphological changes of the median palatine suture in cooperation with Prof. Dr. Dr. Dr. Shahram Ghanaati, Senior Consultant and Head of the Research Laboratory (FORM-Lab, Frankfurt Orofacial Regenerative Medicine-Lab), the Department of Oral and Maxillofacial Surgery of the Goethe-University Frankfurt am Main (Director: Univ.-Prof. Dr. Dr. Robert Sader). Further insights into the transversal resistance of the median palatine sutura should be gained. The working hypothesis says that the age-dependent form changes of the suture, the horizontal and transversal interdigitations (twisting or toothing of the bone suture), respectively, could be responsible for this resistance.
 

Laufzeit: 2017-2022
Projektleiter: Dr. C. Erbe, Univ.-Prof. Dr. Dr. H. Wehrbein

The purpose of this study is to assess the plaque removal efficacy of three experimental manual toothbrushes relative to a regular manual toothbrush using the Turesky Modified Quigley-Hein Plaque Index (TQHPI)

Overall Study Design and Plan
This is a replicate use single brushing, four-treatment, examiner-blind, randomized, eight period, crossover design. Approximately 20 adult subjects at least 18 years of age, will be enrolled into the clinical trial based on study criteria. Subjects will be instructed to refrain from all oral hygiene procedures for approximately 12 hours prior to their appointments. In addition, the subjects will be instructed to refrain from eating, drinking, chewing gum or smoking (including smokeless tobacco) for 4 hours prior to their appointment time. Only small sips of water are permissible. Subjects should refrain from sipping water 45 minutes prior to their scheduled visit.
Inclusion Criteria
In order to be included in the study, each subject must:
-provide written informed consent and receive a signed copy;
-be at least 18 years of age and mainly use a manual toothbrush;
-be in good general health as determined by the investigator/designee based on a review/update of their medical history;
-have a whole mouth average pre-brushing TQHPI score of ³1.75 at Period-1;
-possess a minimum of 16 scorable teeth with facial and lingual scorable surfaces;
-refrain from all oral hygiene procedures for approximately 12 hours prior to this visit and agree to follow this same restriction prior to all visits;
-refrain from eating, drinking (except small sips of water up until 45 minutes prior to their appointment), chewing gum and using tobacco for at least 4 hours prior to this visit and agree to follow these same restrictions prior to all visits;
-agree not to participate in any other oral care study for the duration of this study;
-agree to delay any elective dentistry, including dental prophylaxis, until study completion and to report any non-study dentistry received during the course of this study;
-agree to refrain from using any non-study toothbrushes, dentifrices, mouth rinses, tooth whitening products or floss for the study duration other than their regular at-home toothbrush and toothpaste used between visits;
-agree to maintain their same regular at-home toothbrush and toothpaste for the study duration;
-agree to return for their scheduled visits and to follow all study procedures.Exclusion Criteria
Subjects are excluded from study participation where there is evidence of:
-Any carious lesions requiring restorative treatment;
-active treatment for periodontitis;
-active orthodontic therapy, and/or have removable denture prosthesis;
-any disease or conditions that could be expected to interfere with examination procedures or with the subject safely completing the study (including allergies to dyes);
-dental prophylaxis any time within the 4 weeks prior of the first visit;
-peri/oral piercings;
-using any antibiotics or a chlorhexidine mouth rinse any time within the 2 weeks prior to this visit. 
 

Laufzeit: 2016-2022
Projektleiter: Dr. Christina Erbe, Univ.-Prof. Dr. Dr. H. Wehrbein

"Stain", Clinical Study Agreement Procter & Gamble 2017166

This is a single-center, unsupervised use, single-treatment study. The study will consist of an up-to 3-week stain induction phase followed by a 3-week treatment (stain removal) phase.
A sufficient number of subjects will be screened to obtain approximately 35 adult volunteers to enroll in the study and begin the 3-week run-in phase. Subjects with existing natural tooth stain will receive an optional dental prophylaxis at the beginning of the study, and will be assigned an acclimation toothbrush and toothpaste, and will rinse with tea solution three times daily and with a chlorhexidine rinse (0.1%) once daily for up to three weeks during the run-in phase.
After the run-in phase, up to 30 qualified subjects (with visible stains on anterior teeth) will continue the study and receive treatment products (whitening toothpaste and regular manual toothbrush) to use twice daily for the 3 weeks treatment phase. Tooth color measurements using DIA will be assessed after stain induction (Baseline) and after 3 weeks of treatment (Week 3). Clinical documentary images will be taken at Baseline and Week 3 visits. Subjects will receive a refresher on their oral hygien e instructions at Visit 4 (Week 1).
 

Laufzeit: 2017-2023
Projektleiter: Prof. Dr. Christina Erbe, Dr. Priscila Ferrari Peron, Dr. Ambili Roselina Mundethu

A clinical evaluation of plaque detection by a newly developed QLF (Quantified Light-Induced Fluorescence) based technology

Dental plaque is a causative factor for oral diseases and thus its removal and control are an important aspect of oral health maintenance. Young and fresh plaque that has adhered to the
surface for a short time has a little pathogenicity, but old and mature dental plaque (for example by a lack of oral hygiene) can cause plaque-associated disease such as gingivitis. Therefore, it is clinically important to monitor the progression of plaque accumulation with respect to its age and its degree of coverage on dental surfaces.Since dental plaque is hard to be observed by the naked eye, it is usually disclosed with a staining agent that allows visual identification in dental plaque assessment. More recently, a novel technology has been developed and applied to optically assess dental plaque without a disclosing agent. Quantitative Light-induced Fluorescence (QLF) is an optical method to detect porphyrin
caused red-fluorescence occurring in plaque bacteria which are contributing or adhering to caries (including early white spot lesions), tartar, fluorosis and others. QLF is a light-based, noninvasive, nondestructive, and subject compliant method without the need of using any disclosing agent. The objective of this study is to evaluate a newly developed QLF- and AI- (Artificial Intelligence) based intra-oral camera, called “oral scanner” and compare it to a modified examiner-based index measuring plaque.
One key difference between this oral scanner and market known QLF-based devices, like Qraycam from Inspektor/Aiobio, is the newly developed AI (Artificial Intelligence) algorithms. These
algorithms, running on a smartphone, wirelessly connected to the oral scanner, will enable to automatically identify and record areas of porphyrin based red fluorescence that can signal the occurrence of plaque (from young/fresh to old/mature), enamel ecalcification/white spot lesions, remineralized caries at the fissures and accessory cusps, tartar and fluorosis. A clinical assessment should evaluate the same clinical endpoints by the use of standardized clinical methods allowing a comparison between the oral scanner reads and the clinical assessment. In contrast to former known and published studies (e.g., C. Ganss: Red fluorescence of plaque in the dentition-a comparison of Quantitative Light-induced Fluorescence-Digital (QLF-D) images and conventional images of disclosed plaque) using a QLF device were limited to assess the vestibular surfaces of front teeth, this study will assess all teeth in the mouth from all sides enabled by the use of the oral scanner. In addition to the assessment done with the oral scanner and by the clinical professional, subject’s teeth will be digitally captured/recorded by use of the Primescan AC device from Dentsply Sirona as a reference. This is a non-randomized, single-center, supervised use, observational pilot study with two visits in total: One screening and one study visit. 50 adult and adolescent (13+) subjects who meet inclusion criteria will be enrolled in this study. The reason why adolescents (13+) are enrolled in this clinical study is due to a high likelihood of showing white spot lesions after completing orthodontic treatment with fixed brackets.An oral examination (OST) will be assessed at screening and at visit one. Screening should evaluate if subjects present at least two of the following focused clinical endpoints, while one of those must be plaque:

- plaque (any age of plaque, from young/fresh to old/mature)
- demineralized enamel/white spot lesions
- remineralized caries at the fissures and accessory cusps
- caries
- tartar
- fluorosis

At visit one, an evaluation will be made for each of the available endpoints assessed by a trained dental professional, and the detection and visualization using the QLF-AI-based oral scanner. For
the assessment of plaque subjects will be instructed to refrain from all oral hygiene procedures for approximately 24 hours prior their appointment. The examiner will assess the oral conditions. Then subjects will be asked to use the oral scanner to scan their teeth on their own once before the dental professional scans the subject’s teeth. Additionally, subject s’ teeth will be scanned/captured twice by the use of a professional 3D dental scanner “Primescan AC".

Laufzeit: 2022-2025
Projektleiter: Prof. Dr. Christina Erbe, Dr. Priscila Ferrari Peron, Dr. Ambili Roselina Mundethu

A Clinical Evaluation to Compare a Power Toothbrush Kit to a Manual Toothbrush in the Reduction of Plaque and Gingivitis among a TEENAGER Population with fixed Orthodontic Appliances

The objective of this study is to evaluate and compare the efficacy of an electric toothbrush kit versus a manual toothbrush in the reduction of dental plaque among a population aged 13-19 years with fixed orthodontic appliances over a 12-week period using the Turesky Modified Quigley-Hein Plaque Index. Secondary objective is to assess the reduction of gingivitis using the Löe Silness Gingival Index. This is a single-center, examiner-blind, 12-week, 2 treatment, parallel group, randomized study design. Sixty (60) subjects, between 13-19 years of age, who show evidence of dental plaque and gingivitis and who are routine manual toothbrush users will be enrolled in this study. Plaque measurements will be taken at: Baseline visit (pre- and post-brushing), Week 6, and Week 12 visits (pre-brushing only). Gingivitis measurements will be taken at: Baseline, Week 6, and Week 12 visits. The individual appointments at Baseline, Week 6, and Week 12 will be scheduled for approximately the same time for all visits. Subjects will be instructed to abstain from any oral hygiene for 12 hours prior to all visits.









 

Laufzeit: 2022-2025
Projektleiter: Prof. Dr. Christina Erbe, Dr. Priscila Ferrari Peron, Dr. Ambili Roselina Mundethu

A Clinical Evaluation to Compare a Power Toothbrush to a Manual Toothbrush in the Reduction of Plaque and Gingivitis among a Population with fixed Orthodontic Appliances

The objective of this study was to evalute and compare the efficacy of an electric toothbrush versus a manual toothbrush in the reduction of dental plaque among a gereral population with fixed orthodontic appliances over a 12-week period using the Turesky Modified Quigley-Hein Plaque Index (TQHPI). Secondary objective was to assess the reduction of gingivitis using the Löe Silness Gingival Index (LSGI). This was a single-center, examiner-blind, 12-week, 2 treatment, parallel group, randomized study design. Sixty(60) subjects, at least 13 years of age, who showed evidence of dental plaque and gingivitis and who were routine manual toothbrush users were enrolled in this study. Plaque measurements were taken at: Baseline visit (pre- and post-brushiing), Week 6, and Week 12 visits (both pre-brushing only). Gingivitis measurements were taken at: Baseline, Week 6, and Week 12 visits. The individual appointments at Baseline, Week 6 and Week 12 were scheduled fpr approximately the same daytime for all three visits. Subjects were instructed to abstain from any oralö hygiene for 12 hours prior to all visits.

Laufzeit: 2022-2025
Projektleiter: Dr. Christina Erbe, Univ.-Prof. Dr. Dr. Heiner Wehrbein, Dr. Charlene Ecker

Analyse okklusaler Kontakte durch den P-Scan: Validität und Reliabilität eines Bissanalyseverfahrens

Ein kostengünstiges und schnelles Verfahren zur Bissanalyse ist der P-Scan nach Prodinger-Glöckl. Er besteht aus einem hufeisenförmigen drucksensitiven Artikulationspapier und einem dazu kongruenten Vliespapier, die übereinander gelegt und mittels Bissgabel im Patientenmund positioniert werden. In einem ersten Schritt untersucht die Studie die Validität und Reliabilität des P-Scan zunächst in vitro, um den Nutzen für die klinische Anwendung zu überprüfen. In einem zweiten Schritt werdn die Reproduzerbarkeit der okklusalen Kontakte, die Validität und Reliabilität des P-Scan zur Ermittlung der individuellen Okklusionsverhältnisse anhand von in vivo Untersuchungen an Probanden bei maximaler Interkuspidation überprüft. Anschließend wird ein einem dritten Schritt der P-Scan herangezogen, um die Okklusionsverhältnisse von Patienten mit Craniomandibuläerer Dysfunktion vor und nach osteopathischer Behandlung zu beurteilen und den klinischen Nutzen dieser Methode zu bewerten.

Laufzeit: 2017-2023
Projektleiter: Prof. Dr. Christina Erbe, Dr. Priscila Ferrari Peron, Dr. Ambili Roselina Mundethu

Randomized controlled study to assess performance of two ClearCorrect Clear Aligner staging schedules using digital PAR scores

This study is comparing a two-week aligner stage treatment to a one-week aligner stage treatment over a period of maximum six months by quantifying the performance of the treatment with the digital PAR score. Participants will be randomly assigned to either Group A (two-week schedule) or Group B (one-week schedule), all stratified by the pre-treatment scores and gender. No blinding is possible. Treatment is planned and defined by a trained dental technician together with the prescribing doctor (investigator). All participants will get their set of aligners according their allocated treatment plan. Therefore, number of aligners, as well as the procedure of the teeth movement is individually adjusted and differs from patient to patient. The following three follow-up visits are planned:
- 4 week
- 12 week
- 6 months
The digital Pre- and post-PAR score will be compared for each participant and group. The score will be used to confirm performance and safety of both treatment strategies with the 3-layser aligners. The perceived treatment outcomes will be correlated to the dentition status and by recording patient reported outcome measures (PROMs), the treatment quality will be confirmed from the patient perspective. The digital PAR will be assessed by an independent assessor. The study will show safety by comparing all AEs for both treatment schedules and by assessing the following secondary outcome parameters:
- External Apical Root Resorption (EARR)
- Gingival recession
- Loss of periodontal support
The sample size calculation is based on the publication of Graf et al (2021), assuming a mean change in PAR Index for the one week aligner group of 17.54 with a SD of 6.83 and considering a tolerance range of 3.9 points for the test. Showing non-inferiority for a power of 80% for a test of clinical equivalence a sample size of 35 individuals per group would be needed. Assuming a drop-out rate of 20%, this study aims to recruit 84 patients.Given that the data is normally distributed, primary Outcome will be statistically assessed using a one-tailed T-Test, with a significance level set at α=0.05. Otherwise, a non-parametric test will be applied.Secondary Outcomes will be quantitatively described by means and standard deviations. Differences between the two groups will be tested using Wilcoxon-Rank-Sum tests with a significance level set at α=0.05.




 

Laufzeit: 2022-2025
Projektleiter: Dr. Susanne Wriedt, Univ.-Prof. Dr. Dr. H. Wehrbein

Prospektive Studie zur Untersuchung der Lebensqualitöät von Müttern innerhalb des ersten Jahres nach der Geburt eines Kindes mit Lippen-Kiefer-Gaumenspalte, Ethikkommission der LÄK Rheinland-Pfalz 837.055.17 (10889)

Projektskizze: Das Ziel der geplanten multizentrischen Studie ist die prospektive Einschätzung der mütterlichen Lebensqualität, des Kohärenzgefühls und der sozialen Unterstützung nach der Geburt eines Kindes mit Lippen-Kiefer-Gaumenspalte. Der zu erfassende Zeitraum des ersten Lebensjahres stellt unserer Erfahrung nach für die betroffenen Eltern eine enorme Belastung dar. Auch weisen Vorbefunde auf die massive Belastung der Eltern von Kindern mit LKG-Spalte hin. Diese gerade für die Entwicklung der Mutter-Kind-Beziehung sensible Phase der ersten zwölf Lebensmonate wird durch die schwere Gesichtsfehlbildung von Kindern mit LKG-Spalten erheblich gestört.
Um Änderungen der mütterlichen Lebensqualität innerhalb des ersten Lebensjahres des Kindes zu erfassen, werden die Daten zu drei verschiedenen Messzeitpunkten erhoben. Zusätzlich erfolgt ein Vergleich mit einer Kontrollgruppe. Hierfür werden Mütter, die ein gesundes Kind zur Welt gebracht haben befragt. Der Vergleich soll mögliche Unterschiede der beiden Gruppen aufzeigen.
Die gesammelten Daten werden zur Analyse des Behandlungsablaufes sowie zur Einschätzung der Versorgungssituation der betroffenen Mütter herangezogen.
Studienleiter: OÄ Dr. Karin Strobel, Dr. Ksenija Belaja, Dr. Theodor Klinker; Kieferorthopädie des Universitätsklinikums Erlangen
Prospektive Studie
 

Laufzeit: 2017-2024
Projektleiter: Dr. Susanne Wriedt, Univ.-Prof. Dr. Dr. Heiner Wehrbein, Chrysa Divanidou

Weitere Etablierung der intersisziplinären AKLKG-Datenbank an der Unimedizin Mainz unter Berücksichtigung der 3D-Datensätze DVT, Gesichts- und Modellscan

Nach Überprüfung der Datenbankabfrage für MKG und KFO und der digitalen Gesichtserfassung und Modellerstellung bezüglich Validität und Reliabilität sollehn nun die Erhebung der Befunde laufender und die Archivierung der Befunde beendeter Behandlungen digitalisiert und anschließend mit schon digital archivierten Daten von Patienten mit LKG-Spalten zusammengeführt werden. Es handelt sich momentan um eine Gruppe von ca. 800 Patienten. Das Ziel ist eine bessere Auffindbarkeit der interdisziplinär erstellten Behandlungsunterlagen zur Verbesserung der Behandlung des einzelnen Patienten (Vernetzung der einzelnen Kliniken) und die Verwendbarkeit der Daten für Multicenter-Studien (wie vom AKLKG intendiert, z. B. German Cleft Network Studie zur prächirurgischen Therapie), sowie zur Verbesserung der Behandlung zukünftiger Patienten (Versorgungsforschung). Durch die digitale Aufbereitung der Unterlagen werden Platzprobleme für Akten- und Modellarchive beseitigt (Papierlose Klinik)

Literatur:
Wriedt Susanne, Foersch Moritz, Muhle Jan Daniel, Schmidtmann Irene, Wehrbein Heinrich. Multibracket appliance: impression defaults and their reduction by blocking-out - a three-dimensional study. CLINICAL ORAL INVESTIGATIONS 2016; 20 (2): 365-372
Wriedt Susanne, Schmidtmann Irene, Niemann Mareike, Wehrbein Heinrich. Digital 3D image of bimaxillary casts connected by a vestibular scan. JOURNAL OF OROFACIAL ORTHOPEDICS-FORTSCHRITTE DER KIEFERORTHOPADIE 2013; 74 (4): 309-318

Laufzeit: 2016-2024

Publikationen

Bulski Julia Camila, Schulz-Weidner Nelly, Freudenberg Andrea
Autoren der Einrichtung: Bulski Julia Camila
Lückenschluss nach Extraktion von sechsjährigen Molaren mit Molaren-Schneidezahn-Hypomineralisation unterstützt durch das myofunktionelle kieferorthopädische Therapiekonzept "mykie" - ein Fallbericht
Informationen aus Orthodontie und Kieferorthopädie. 2022; 0020-0336 (1439-4200): 243-250

Erbe Christina, Crismani Adriano
Autoren der Einrichtung: Erbe Christina
Interview with Univ.-Prof. Dr. Christina Erbe, Director of the Department of Orthodontics, University Medical Center Mainz (26.07.2022)
INFORMATIONEN AUS ORTHODONTIE UND KIEFERORTHOPAEDIE. 2022; 54 (03): 205-207 Editorial Material
Datensatz in Web of Science®

Erbe Christina, Heger Sarah, Kasaj Adrian, Berres Manfred, Wehrbein Heinrich
Autoren der Einrichtung: Erbe Christina, Heger Sarah, Wehrbein Heinrich
Weitere Autoren des Fachbereichs: Kasaj Adrian, Berres Manfred
Orthodontic treatment in periodontally compromised patients: a systematic review
CLINICAL ORAL INVESTIGATIONS. 2022; 27 (1): 79-89 Review
Datensatz in Web of Science®

Hitti Mirette, Welte-Jzyk Claudia, Proebster Lothar, Erbe Christina
Autoren der Einrichtung: Hitti Mirette, Welte-Jzyk Claudia, Erbe Christina
CMD and orthodontics
INFORMATIONEN AUS ORTHODONTIE UND KIEFERORTHOPAEDIE. 2022; 54 (04): 221-228 Article
Datensatz in Web of Science®

Holzgreve Fabian, Fraeulin Laura, Betz Werner, Erbe Christina, Wanke Eileen M., Brueggmann Doerthe, Nienhaus Albert, Groneberg David A., Maurer-Grubinger Christian, Ohlendorf Daniela
Autoren der Einrichtung: Erbe Christina
A RULA-Based Comparison of the Ergonomic Risk of Typical Working Procedures for Dentists and Dental Assistants of General Dentistry, Endodontology, Oral and Maxillofacial Surgery, and Orthodontics
SENSORS. 2022; 22 (3): Article
Datensatz in Web of Science®

Holzgreve Fabian, Fraeulin Laura, Maurer-Grubinger Christian, Betz Werner, Erbe Christina, Weis Tim, Janssen Keno, Schulte Lisa, de Boer Amaya, Nienhaus Albert, Groneberg David A., Ohlendorf Daniela
Autoren der Einrichtung: Erbe Christina
Effects of Resistance Training as a Behavioural Preventive Measure on Musculoskeletal Complaints, Maximum Strength and Ergonomic Risk in Dentists and Dental Assistants
SENSORS. 2022; 22 (20): Article
Datensatz in Web of Science®

Lorenz J., Schidtmann I, Morawietz M., Kiesow A., Wehrbein H., Sarembe S., Erbe C.
Autoren der Einrichtung: Lorenz J., Wehrbein H., Erbe C.
In vitro surface analysis of the brushing resistance of orthodontic sealants using two different profilometric evaluation methods
SCIENTIFIC REPORTS. 2022; 12 (1): Article
Datensatz in Web of Science®

Sauer Mareike Kristin, Drechsler Thomas, Peron Priscilla Ferrari, Schmidtmann Irene, Ohlendorf Daniela, Wehrbein Heinrich, Erbe Christina
Autoren der Einrichtung: Sauer Mareike Kristin, Peron Priscilla Ferrari, Wehrbein Heinrich, Erbe Christina
Weitere Autoren des Fachbereichs: Schmidtmann Irene
Aligner therapy in adolescents: first-year results on the impact of therapy on oral health-related quality of life and oral hygiene
CLINICAL ORAL INVESTIGATIONS. 2022; 27 (1): 369-375 Article
Datensatz in Web of Science®

Weitbrecht Moritz, Holzgreve Fabian, Fraeulin Laura, Haenel Jasmin, Betz Werner, Erbe Christina, Maurer-Grubinger Christian, Wanke Eileen M., Brueggmann Doerthe, Nienhaus Albert, Groneberg David A., Ohlendorf Daniela
Autoren der Einrichtung: Erbe Christina
Ergonomic Risk Assessment of Oral and Maxillofacial Surgeons - RULA Applied to Objective Kinematic Data
HUMAN FACTORS. 2022: Article
Datensatz in Web of Science®

Auswahl an wissenschaftlichen Vorträgen

Prof. Dr. Christina Erbe
Dentalfotografie - Wichtige Dokumentation
Zahnheilkunde 2022 - Bestens verzahnt am 01.+02.04.2022 in Mainz

Prof. Dr. Christina Erbe
Offener Biß - und nun?
7. Wissenschaftskongress der Deutschen Gesellschaft für Aligner Orthodontie vom 18.-19.11.2022 in Köln

Prof. Dr. Christina Erbe
Spektrum der Alignertherapie
30. Wintersymposium - Kieferorthopädie und Kinderzahnmedizin für die tägliche Praxis vom 15.-20.01.2022 in Going/Tirol

Dr. Priscila Ferrari Peron
Clinical Parameters and inflammatory biomarkers among patients with brackets
97th Congress of the European Orthodontic Society vom 31.05.-03.06.2022 in Limassol/Cyprus

Dr. Priscila Ferrari Peron
Quantitative Analyse von White Spot Läsionen während der Behandlung mit Multibracket-Apparatur: Ein In-vivo-Vergleich
94. Jahrestagung der Deutschen Gesellschaft für Kieferorthopädie vom 21.-24.09.2022 in Berlin

Dr. Ambili Roselina Mundethu
Altersabhängige Gefäßdichte im humanen parodontalen Ligament - Eine histomorphometrische Studie
94. Jahrestagung der Deutschen Gesellschaft für Kieferorthopädie vom 21.-24.09.2022 in Berlin

Dr. Ambili Roselina Mundethu
Debonding Polycrystalline ceramic brackets mittels Er,Cr:YSGG laser
54. Jahrestagung der Arbeitsgemeinschaft für Grundlagenforschung (Afg) am 14.01.2022 in Mainz

Dr. Susanne Wriedt
Funktions- und Kieferstatus bei Kindern und Erwachsenen mit Achondroplasie
Jahrestreffen des "Bundesverbandes kleinwüchsiger Menschen und ihre Familien" vom 26.-28.05.2022 in Hausen

Dr. Susanne Wriedt
Kieferorthopädie mit Schwerpunkt Funktion und Frühbehandlung
Eltern- und Betroffenenseminar der AG Silver-Russel-Syndrom (SRS), Small für Gestational Age (SGA) und Wachstumshormonmangel (WHM) des BKMF e.V. vom 16.-17.09.2022 in Hausen

Promotionen

Frederic Johann Werner Fuchs
Visuelle Wahrnehmung des Mundhygienestatus mit Eye-Tracking von Patienten mit Multibracket-Apparatur durch Jugendliche, Erziehungsberechtigte und Studierende der Zahnmedizin - Eine Pilotstudie

Mirette Christin Hitti
Vergleichende retrospektive, kephalometrische Untersuchung zur Therapie mit Alignern versus Herbst-Apparatur

Julian Karl Textor
Halitosis und Lebensqualität bei Jugendlichen mit verschiedenen kieferorthopädischen Apparaturen

Verschiedene wissenschaftliche Aktivitäten

Preise

Dr. Ambili Roselina Mundethu
Preis der Lehre für Fachbereich 04