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Surgical Treatment of Peri-implantitis Using a Bone Substitute With or Without a Resorbable Collagen Membrane
Sponsor: Andrea Ravida
Summary
The objective of the present randomized clinical trial will be to compare two surgical methods of treating peri-implantitis. This study will determine if surgical debridement of peri-implantitis bone defects, including air powder abrasive (APA) decontamination of implant surfaces, in combination with the placement of a bone graft, differs in treatment outcomes compared to placing the same bone graft material with a resorbable collagen membrane placed over the bone graft.
Official title: Surgical Treatment of Peri-implantitis Using a Bone Substitute With or Without a Resorbable Collagen Membrane. A Randomized Clinical Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
52
Start Date
2023-01-30
Completion Date
2028-12
Last Updated
2026-02-17
Healthy Volunteers
Yes
Conditions
Interventions
InterOss Collagen (Bone xenograft) and InterOss Collagen Guide (Collagen membrane)
Group will receive InterOss Collagen and InterOss Collagen Guide during surgical intervention visit.
InterOss Collagen (Bone xenograft)
Group will only receive InterOss Collagen during surgical intervention visit.
Locations (1)
University of Pittsburgh School of Dental Medicine
Pittsburgh, Pennsylvania, United States