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Making skeletal class III malocclusion treatment more effective by using a facemask and a modified skeletal expander

Effectiveness of buccal and labial pads addition in improving the efficiency of skeletal class III malocclusion treatment using face mask appliance combined with rapid maxillary expansion: a randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN20427295
Enrollment
40
Registered
2023-01-24
Start date
2023-04-01
Completion date
Unknown
Last updated
2024-02-12

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

Conditions

Skeletal class III and maxillary transverse deficiency. Oral Health

Interventions

Patients will be randomly allocated into two groups using Microsoft® Excel electronic randomization: Arm 1: Experimental group: Each Patient in this group will be treat

Sponsors

Damascus University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Skeletal class III caused by maxillary deficiency with or without mandibular prognathism. 2. Maxillary transverse deficiency. 3. Patients with normal or horizontal growth patterns. 4. Patients in early mixed dentition (7-10 years old).

Exclusion criteria

Exclusion criteria: 1. Patients with syndromes or craniofacial abnormalities. 2. Patients with vertical growth patterns. 3. Poor oral hygiene. 4. Previous orthodontic treatment.

Design outcomes

Primary

MeasureTime frame
1. Sagittal and vertical skeletal changes before and after treatment will be assessed using cone-beam computed tomography-generated cephalograms. 2. Dentoalveolar changes including: 2.1. Upper incisor angle changes. 2.2. The permanent maxillary first molar inclination changes. 2.3. Height and thickness of alveolar bone. Dentoalveolar changes before and after treatment will be assessed using cone-beam computed tomography.

Secondary

MeasureTime frame
1. Soft tissue changes before and after treatment will be assessed using profile photography. 2. Levels of pain and discomfort measured using a questionnaire given to the patients.

Countries

Syria

Outcome results

None listed

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