Evaluating changes in teeth after surgical extrusion treatment
Surgical Extrusion: Volumetric and Insertion Analysis at 6 Months. Series of 10 Cases
Aula Dental Avanzada · NCT05201664
This study is testing how surgical extrusion treatment affects the position and health of teeth and surrounding tissue in patients who choose this option instead of extraction or implants.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 15 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Aula Dental Avanzada (other) |
| Locations | 1 site (Alicante) |
| Trial ID | NCT05201664 on ClinicalTrials.gov |
What this trial studies
This observational study aims to clinically evaluate the changes in teeth that have undergone surgical extrusion treatment. It will assess three key parameters: the position and volume of the soft tissue, and the level of periodontal attachment before and six months after the treatment. Data will be collected through intraoral scanning and periodontal probing, with statistical analysis performed to draw conclusions about the effectiveness of the surgical extrusion approach. The study focuses on understanding the outcomes of this treatment method for patients who prefer it over extraction or implants.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with a tooth that has a subgingival residual dentine margin and who refuse extraction or dental implants.
Not a fit: Patients who may not benefit include those with contraindications for surgical intervention or those with teeth that have vertical fractures or significant periodontal issues.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of surgical extrusion as a viable alternative to tooth extraction.
How similar studies have performed: While there may be limited data on surgical extrusion specifically, similar approaches in dental treatments have shown promise, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Tooth with a subgingival residual dentine margin. * Patients refusing tooth extraction and dental implant placement as first choice. Exclusion Criteria: * Patients in whom surgical intervention is contraindicated. * Teeth with vertical fractures up to the apex. * Teeth with pocket depth \>4 mm in any of their walls. * Failure of the treatment leading to the loss of the extruded tooth.
Where this trial is running
Alicante
- Clínica Dental esteve — Alicante, Spain (RECRUITING)
Study contacts
- Study coordinator: Guillem Esteve-Pardo, DDS
- Email: guillem@clinicaesteve.es
- Phone: +34 965215755
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.
Conditions: Tooth Extruded, Tooth Extrusion, Tooth Avulsion, Tooth Fracture, surgical extrusion, oral surgery, tooth extrusion