20-25 Year Follow-Up on Regenerative Bone Procedures for Peri-Implantitis
Condition(s) studied
Investigational drug(s) / intervention(s)
Bone regenerative surgery with a bone graft substitute and a resorbable membrane: Dental implants with a diagnosis peri-implantitis were treated with regenerative surgery.
Study 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.
Eligibility
Primary outcome measure(s)
- Bone fill — Ten years after surgical regenerative boneprocedures
Radiographic bone fill measured mesial and distal at the implant on an intra oral radiograph. Measurements will be performed by a blinded radiologist.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Kristianstad Univeristy | Kristianstad | Sweden |
More Kristianstad University trials in Sweden
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06648564 on ClinicalTrials.gov ↗ ← All trials in Sweden