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Regenerative Treatment of Peri-implantitis

NCT06153212 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2026-01-29

No results posted yet for this study

Summary

The purpose of this study is to study the use of a new type of d-PTFE membrane called reinforced PTFE Mesh (RPM) with dental surgery. The regenerative outcomes of RPM membranes and collagen membrane for surgical reconstructive treatment of peri-implantitis (gum disease around implants) will be compared.

Conditions

  • Peri-Implantitis

Interventions

PROCEDURE

Membrane placement with bone grafting

The diseased dental implant will be cleaned and the bone defect will be filled with bone graft and covered by a membrane.

Sponsors & Collaborators

Principal Investigators

  • Muhammad Saleh, BDS, MSD · University of Michigan

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-02
Primary Completion
2026-06-01
Completion
2026-12-01

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06153212 on ClinicalTrials.gov