Comparing Damon Ultima and Conventional Brackets for Orthodontic Treatment
Clinical Effectiveness of Damon Ultima Vs Conventional Brackets (A Randomized Clinical Trial)
This study is testing whether the Damon Ultima braces work better and cause less pain than traditional braces for people with certain types of teeth crowding.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 34 (estimated) |
| Ages | 15 Years to 35 Years |
| Sex | All |
| Sponsor | University of Baghdad Academic / other |
| Locations | 1 site (Baghdad) |
| Trial ID | NCT05978817 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effectiveness of the Damon Ultima orthodontic system against conventional brackets in treating skeletal and dental Class I malocclusion with moderate crowding. The study will evaluate clinical performance, root resorption, and pain perception associated with each bracket type. The Damon Ultima system is designed for enhanced precision and faster treatment outcomes through its innovative bracket design and specially engineered archwires. Participants will be monitored throughout the treatment process to assess these parameters.
Who should consider this trial
Good fit: Ideal candidates are healthy individuals aged 15-35 with Class I malocclusion and moderate dental irregularity who have not undergone previous orthodontic treatment.
Not a fit: Patients with severe skeletal discrepancies requiring surgery, or those with conditions like cleft lip or palate, will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved orthodontic treatment outcomes with less pain and better control over tooth movement.
How similar studies have performed: Previous studies have shown promising results with self-ligating brackets, suggesting potential benefits in treatment efficiency and patient comfort.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 15-35 years of age patients who are healthy and without medications such as non-steroidal anti-inflammatory analgesics. * Patients with Class I normal occlusion with moderate dental irregularity (with 4-6 irregularity index) requiring non-extraction treatment. * Presence of all the permanent teeth apart from the third molars. * Patients with good oral hygiene and periodontal health. * Without previous orthodontic treatment/ functional appliances Exclusion Criteria: Patients will be excluded from recruitment if he had sever skeletal discrepancy that requires orthognathic surgery. • Patients who have cleft lip or palate, hypodontia, or hyperdontia
Where this trial is running
Baghdad
- Nawar A jebory — Baghdad, Iraq (Recruiting)
Study contacts
- Principal investigator: Dheaa H Al-Groosh, PHD — University of Baghdad
- Study coordinator: Nawar A jebory, PHD student
- Email: nooorznawar@gmail.com
- Phone: 07809752102
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.