Clinical, Radiographic, and Digital Evaluation of the Effects of Autogenous Grafts on Peri-implant Mucosa
Condition(s) studied
Investigational drug(s) / intervention(s)
Coronal palatal tissue: This group will receive palatal grafts including marginal and interdental gingiva. This coronal palatal tissue will be applied to the peri-implant tissue at the second-stage implant surgery.
Apical palatal tissue: This group will receive palatal grafts harvested from approximately 1.5 mm apical to the gingival margin. This graft will be applied to the peri-implant tissue at the second-stage implant surgery.
Study summary
This study aims to evaluate the effects of autogenous grafts harvested from different palatal regions on the peri-implant mucosa when applied during second-stage dental implant surgery.
Clinical, radiographic, and digital assessment methods will be used to investigate the early effects of these grafts on peri-implant mucosal width and thickness. In addition, peri-implant tissue health and patient-reported outcomes will be evaluated to compare the effectiveness of the grafting techniques in peri-implant soft tissue management.
Eligibility
Primary outcome measure(s)
- Peri-implant Mucosal Thickness — Pre-operative and post-operative (before implant placement, 3rd month (second-stage implant surgery), 6th month after implant placement, and 12th month after prosthetic loading)
The primary outcome is the change in peri-implant mucosal thickness measured at four time points using clinical and digital methods.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Kutahya Health Sciences University | Kütahya | Merkez | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07330609 on ClinicalTrials.gov ↗ ← All trials in Turkey