Comparing clear aligners and fixed braces for treating mild Class II malocclusion in adults
Evaluation of Efficacy of Clear Aligners in Correction of Class II Malocclusion Using Intermaxillary Elastics: A Randomized Controlled
This study is testing whether clear aligners or traditional braces work better for adults with mild Class II malocclusion to improve their teeth and bite.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 24 (estimated) |
| Ages | 15 Years to 20 Years |
| Sex | All |
| Sponsor | Hama University Academic / other |
| Locations | 1 site (Hama, Hama Governorate) |
| Trial ID | NCT05684510 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of clear aligners with intermaxillary elastics versus traditional fixed multibracket appliances in treating adult patients with mild Class II division 1 malocclusion and increased overjet. Participants will be divided into two groups: one receiving clear aligners and the other receiving fixed appliances. The study will assess changes in skeletal, dental, and soft tissue as a result of each treatment method. The goal is to determine which approach yields better outcomes for patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 15-20 with mild Class II division 1 malocclusion and moderate overjet.
Not a fit: Patients with periodontal disease, vertical growth patterns, or severe skeletal Class II malocclusion may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with a more effective and comfortable treatment option for mild Class II malocclusion.
How similar studies have performed: Previous studies have shown promising results for clear aligners in orthodontic treatment, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * \- Patients with permanent occlusion at age 15-20 years. * Patients with class II division I (half cusp or Less) with moderate overjet (2-4mm). * Patients with normal or horizontal growth pattern. * Mild crowding (\_\<2 mm) in maxillary and mandibular arch. * Patient with satisfactory periodontal health and good oral hygiene * No previous orthodontic treatment * Comprehensive medical and dental history ruling out any systemic disease. Exclusion Criteria: * Patients with periodontal disease. * Patients with vertical growth pattern. * Patients with missing or extracted teeth except third molar. * Patients with temporomandibular joint disorder. * Patients with Skeletal open bite. * Patients with poor oral and gingival health * Patients with neuromuscular disorder. * Patients with severe skeletal class II.
Where this trial is running
Hama, Hama Governorate
- Hama University — Hama, Hama Governorate, Syria (Recruiting)
Study contacts
- Principal investigator: FATIMA NASHTR, MSc — Hama University
- Study coordinator: Fadi Jnaid
- Email: Drfadijnaid@gmail.com
- Phone: 988499015
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.