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Evaluation of the Efficacy of Modified Removable Mandibular Retractor Appliance in the Treatment of Class III Malocclusion (A Clinical Randomized Controlled Trial)

Evaluation of the Efficacy of Modified Removable Mandibular Retractor Appliance in the Treatment of Class III Malocclusion (A Clinical Randomized Controlled Trial) - RCT

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00027155
Enrollment
40
Registered
2021-11-29
Start date
2020-11-09
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angle's class III malocclusion K07

Interventions

Group 1: treatment of children in mixed dentition with skeletal class III and anterior crossbite by modified removable mandibular retractor Group 2: treatment of children in mixed dentition with

Sponsors

Damascus Dental School, Damascus University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 10 Years

Inclusion criteria

Inclusion criteria: 7–10 years of with first permanent molars erupted; Class III molar relationship in the early mixed dentition; • anterior crossbite on two or more incisors with or without mandibular displacement oo Closure skeletal class III relationship judged clinically and confirmed radiographically (– 4<ANB<0), the child should be of a Syrian ancestry.

Exclusion criteria

Exclusion criteria: 1-Severe skeletal class III resulting primarily from mandibular prognathism (ANB less than - 4°) 2. Class III patients with craniofacial syndromes 3. Cleft lip and palate patients 4.previous orthodontic treatment;

Design outcomes

Primary

MeasureTime frame
What? Changes in hard-tissue and soft-tissue How? changes will be assessed using cephalometric radiographs. When? Cephalometric radiographs will be taken before and after treatment. The end point of the trial will be at after the correction of the reversed overjet. Measurements on cephalometric before and after treatment will be compared.

Secondary

MeasureTime frame
pain and discomfort during treatment

Countries

Syria

Contacts

Public ContactAmmar Al-Hammadi

Damascus Dental School, Damascus University

ammarhammadi323@gmail.com00963992875247

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026