- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06935032
Functional Appliance Effects on Mandibular Soft Tissues
Evaluation of Mandibular Soft Tissue Changes in Patients Using Functional Appliances
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This retrospective study aims to investigate the changes in the mandibular and cervical soft tissues of patients with Class II malocclusion and mandibular retrognathia treated with the Twin Block appliance. The study includes patients treated in the Department of Orthodontics, Faculty of Dentistry, XXXX University, between 2021 and 2023. Ethical approval was obtained from the relevant ethics committee (Decision No: 2023/351), and informed consent was secured from all participants and their parents.
A total of 46 individuals were included: 16 patients with Class II Division I malocclusion, 15 with Class II Division II malocclusion, and 15 control subjects with skeletal Class I malocclusion. All patients in the treatment groups were in the growth spurt phase (CVMS3-S4) and received Twin Block therapy full-time for 12 months. The control group received fixed orthodontic treatment without functional appliances.
Profile photographs and lateral cephalometric radiographs were obtained at the beginning of treatment (T1) and after 1 year of therapy (T2), using a standardized protocol in natural head position (NHP). Measurements were performed digitally using Dolphin Imaging software. The study assessed angular parameters such as the submental-facial angle, cervicomental angle, lip-jaw-throat angle, and Sm-E plane angle from photographs, as well as linear measurements from cephalometric radiographs, including throat length, jaw tip contour, soft tissue pogonion thickness, soft tissue menton thickness, and lower lip-pogonion distance.
Sample size was determined via power analysis, which indicated that 15 patients per group were sufficient to detect clinically meaningful differences. To ensure measurement reliability, cephalometric analyses were repeated, and intra-observer reliability was confirmed with an intraclass correlation coefficient (ICC) of 0.924.
Statistical analyses were conducted using R software. Paired t-tests were employed for within-group comparisons, while independent t-tests and ANOVA with Tukey's post hoc tests were used for intergroup comparisons. Mixed-effects models and chi-square tests were utilized where appropriate. A significance level of p < 0.05 was adopted for all analyses.
This study was designed to contribute to the understanding of how Twin Block functional appliance therapy influences the morphology of the mandibular and cervical soft tissues, using both photographic and radiographic assessments in a growing patient population.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Meram
-
Konya, Meram, Turkey, 42090
- Necmettin Erbakan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- having Class II malocclusion caused by mandibular retrognathia (ANB > 4°, SNB<78°),
- exhibiting horizontal and/or normal growth pattern (SN-GoGn=32 ±6),
- having profile photographs and cephalometric radiographs taken in the NHP (using the self-balance method one of the dynamic approaches for determining NHP)15,
- not requiring rapid maxillary expansion,
- not having increased initial lower incisor inclination on lateral cephalometric radiographs,
- Class II Division 2 patients presenting with ≥4 mm deepbite and the absence of any prior upper incisor protrusion methods,
- the control group individuals were required to have a skeletal Class I pattern (ANB angle between 0-4°) without any dental deficiencies.
Exclusion Criteria:
- previous orthodontic treatment,
- presence of craniofacial anomalies involving the jaw and/or teeth,
- severe facial asymmetry
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Class II Division I malocclusion caused by mandibular retrognathia
Class II Division I patients treated with the Twin Block appliance
|
An appliance that facilitates forward positioning of the mandible and soft tissues
|
|
Experimental: Class II Division II malocclusion caused by mandibular retrognathia
Class II Division II patients treated with the Twin Block appliance
|
An appliance that facilitates forward positioning of the mandible and soft tissues
|
|
Experimental: Skeletal Class I patients
Class I patients who received fixed treatment
|
Patients undergoing orthodontic treatment with fixed appliances
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patients treated with the Twin Block appliance
Time Frame: 12 month
|
The changes in certain angular (degrees) and linear (millimeters) measurements may be considered favorable for the mandibular soft tissues.
|
12 month
|
Collaborators and Investigators
Investigators
- Principal Investigator: Seda Sağoğlu, Konya Necmettin Erbaka University Faculty of Dentistry
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/351
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Study Data/Documents
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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