Comparing two methods of dental occlusion measurement in adult orthodontic patients
Quantification of the Differences in the Diagnostic Relationships Between Centric Occlusion Versus Maximum Intercuspation in Adult Orthodontic Patients : A Cross-sectional Study
This study is testing two different ways to measure how teeth fit together in adults getting orthodontic treatment to see which method gives better results.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 13 Years to 30 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06220955 on ClinicalTrials.gov |
What this trial studies
This observational study aims to quantify the differences in diagnostic relationships between centric occlusion and maximum intercuspation in adult orthodontic patients. It utilizes both conventional methods, including semi-adjustable articulators and face bow records, as well as a digital method involving a dental intraoral scanner. The study focuses on various orthodontic relations such as molar, canine, and incisor relations, as well as overjet, overbite, and midline discrepancies. By comparing these methods, the study seeks to enhance the accuracy of orthodontic diagnostics.
Who should consider this trial
Good fit: Ideal candidates for this study are adult orthodontic patients with full permanent dentition.
Not a fit: Patients who have undergone previous orthodontic treatment, syndromic patients, or those with retained primary teeth or heavily restored teeth may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the precision of orthodontic assessments, leading to better treatment outcomes for patients.
How similar studies have performed: While similar studies have explored occlusion measurement methods, this specific comparison of conventional and digital techniques is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: orthodontic patient having full permanent dentition Exclusion Criteria: * patients who had undergone previous orthodontic treatment, and syndromic patients, retained primary teeth , teeth heavily restored
Where this trial is running
Cairo
- faculty of dentistry Cairo university — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: Ghada Elzanaty, BSC
- Email: ghadaelzanatie@gmail.com
- Phone: 01115427427
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.