Clinical Trial

20-25 Year Follow-Up on Regenerative Bone Procedures for Peri-Implantitis

Study acronym: periimpl20y
Enrolling by Invitation
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Summary
The goal of this 20-25-year observational study is to investigate the outcomes of bone regenerative surgery in peri-implantitis. Two different techniques will be compared: surgery with a bone substitute alone and surgery with a bone substitute combined with a membrane, to determine their effectiveness and assess whether one is more effective than the other. The intention of this observational study is to learn more about the long-term effects of bone regenerative surgery in patients with peri-implantitis. Patients will be called in for a clinical and radiographic examination of the surgically treated implant(s). Probing pocket depths, presence of pus, bleeding around the implant (s) and a radiograph of the implant (s). To be able to compare with the 1, 3, 5 and 10 year measurements.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-10-17; most recent amendment 2026-06-24.
Trial Details
NCT Number NCT06648564
Lead Sponsor Kristianstad University
Conditions Peri-implantitis
Enrollment 20 participants
Start Date 2025-08-31
Primary Completion 2026-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-29