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ENROLLING BY INVITATION
NCT05699343
NA

Surgical Treatment of Peri-implantitis Using a Bone Substitute With or Without a Resorbable Collagen Membrane

Sponsor: Andrea Ravida

View on ClinicalTrials.gov

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

Interventions

PROCEDURE

InterOss Collagen (Bone xenograft) and InterOss Collagen Guide (Collagen membrane)

Group will receive InterOss Collagen and InterOss Collagen Guide during surgical intervention visit.

PROCEDURE

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