NCT06354374 Soft Tissue Volume, Dimensions and Tomographic Alveolar Ridge Classification System for Dental Implant Treatment.
| NCT ID | NCT06354374 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ain Shams University |
| Condition | Soft Tissue Volume |
| Study Type | OBSERVATIONAL |
| Enrollment | 350 participants |
| Start Date | 2024-02-22 |
| Primary Completion | 2025-07 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 350 participants in total. It began in 2024-02-22 with a primary completion date of 2025-07.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Despite the importance of soft tissue dimensions for periodontal, restorative, implant, and orthodontic treatment, the current classifications of tomographic alveolar ridge topography lack the soft tissue component(Tolstunov, 2014). Therefore, the present study will be to evaluate the relationship between soft tissue volume and the dimensions \& tomographic alveolar ridge classes as well as to incorporate the soft tissue volumetric evaluation in the classification system.
Eligibility Criteria
Inclusion Criteria: 1. Adult patients in a healthy systemic condition who required comprehensive dental treatment. 2. Both genders with age group \> 18 years old. 3. Patients should have at least a single missing tooth that requires dental implant placement. 4. Healing period of 3 months after extraction prior to surgical procedures. 5. CBCT scans will be obtained as a part of the comprehensive dental treatment. 6. Patients should approve to deliver a signature to a written consent after studying nature explanation. Exclusion Criteria: 1. Patients with severe smoking habits \>10 cig \\ day. 2. Pregnant females, decisional impaired individuals, Prisoners, and handicapped patients. 3. Patients having poor oral hygiene or not wanting to carry out oral hygiene measures. 4. Patients on any medication affecting the soft tissue health (e.g., amlodipine, Cyclosporine A, hydantoin) 5. Patients with infections either periodontally or periapically
Frequently Asked Questions
Who can join the NCT06354374 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Soft Tissue Volume. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06354374 currently recruiting?
Yes, NCT06354374 is actively recruiting participants. Visit ClinicalTrials.gov or contact Ain Shams University to inquire about joining.
Where is the NCT06354374 trial being conducted?
This trial is being conducted at Al Shorouk City, Egypt.
Who is sponsoring the NCT06354374 clinical trial?
NCT06354374 is sponsored by Ain Shams University. The trial plans to enroll 350 participants.