Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation
NCT: NCT07679451 · RECRUITING
Brief Summary
This randomized controlled clinical study aims to evaluate and compare the effectiveness of custom-made polyether ether ketone (PEEK) membranes versus polytetrafluoroethylene (PTFE) membranes in guided bone regeneration for maxillary alveolar ridge augmentation in the esthetic zone. Thirty patients requiring ridge augmentation prior to dental implant placement will be enrolled and randomly allocated into two equal groups. Group A will receive customized PEEK membranes, while Group B will be treated with PTFE membranes. Clinical and radiographic assessments, including cone beam computed tomography (CBCT), will be performed immediately postoperatively, at 6 months, and at 12 months to evaluate volumetric, horizontal, and vertical bone gain as well as soft tissue healing and complication rates.
Frequently Asked Questions
What is Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation?
Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation is a clinical trial registered under NCT07679451. Current status: RECRUITING.
What is the status of NCT07679451?
The current status of NCT07679451 (Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation) is: RECRUITING.
When did Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation start?
Custom-Made PEEK Versus PTFE Membranes in Maxillary Alveolar Ridge Augmentation started on 2026-01-01.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.