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

NCT06648564 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2025-02-13

No results posted yet for this 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.

Conditions

  • Peri-implantitis

Interventions

PROCEDURE

Bone regenerative surgery with a bone graft substitute and a resorbable membrane

Dental implants with a diagnosis peri-implantitis were treated with regenerative surgery.

Sponsors & Collaborators

  • Kristianstad University

    lead OTHER

Principal Investigators

  • AM R Jansaker, Ass.Prof. · Malmö University

  • Stefan Renvert, Prof. · Kristianstad University

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-31
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Sweden

Study Locations

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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 NCT06648564 on ClinicalTrials.gov