CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 38 enrolled
Drug / intervention
Chincup +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05350306
NCT05350306N/ACompleted
CompareCT.gov

Evaluation of the Dimensional Changes in the Mandible, Condyles, and the Temporomandibular Joint Following Skeletal Class III Treatment With the Chin Cup Using Low-Dose Computed Tomography

Damascus University·interventional·Posted Apr 28, 2022·Updated May 4, 2022

In Brief

A clinical study evaluating Chincup and Control group for Class III Malocclusion. Completed, enrolled 38 participants across 1 site.

Detailed Summary

This in vivo comparative study will evaluate the changes in the mandibular dimensions and the glenoid fossa after skeletal class III subjects' therapy by chincup appliance and compare it with an untreated class III control group. Pre and post-treatment low-dose computed tomography images will be taken before and after achieving positive overjet and undergoing 16 months of active treatment/ observation. Dimensional and volumetric changes in the mandible, condyles, and glenoid fossa will be calculated and compared to those observed in the control group.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsClass III Malocclusion
CountriesSyria
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedApr 28, 2022
Enrollment StartJan 1, 2019
Primary CompletionJan 1, 2022
Study CompletionApr 1, 2022
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 4.2 years ago

Interventions

Chincupdevice

Patients will receive an individual fabricated bonded bite block and occipital chincup. A 400-500g/side retroactive force will be applied in the direction of the condyles. Patients or panthers will be instructed to wear the appliance /14-16/ hours a day.

Control groupother

The changes in condyle-mandibular volumes and superficial areas and relative positions of the condyles and glenoid fossa will be calculated after 16 months of observation.