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10 Year Follow-up on Reconstructive Bone Procedures for Peri-implantitis

NCT07678892 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2026-07-02

No results posted yet for this study

Summary

The purpose of this 10 year observational follow-up study was to evaluate the long-term outcomes of reconstructive surgical treatment of peri-implantitis. Two treatment approaches have been compared using a bone substitute with or without a resorbable membrane.The objective was to assess their effectiveness and determine wheter one treatment strategy provided superior long-term outcomes.

Participants were invited for clinical and radiographic examinations of the previously treated implant. Clinical assessments included probing pocket depth measurements, evaluation of bleeding on probing, presence of suppuration, and radiographic assessment of peri-implant bone levels.

Conditions

  • Peri-Implantitis

Interventions

PROCEDURE

Treatment with a bone graft and a membrane

Dental implants with a diagnosis of peri-implantitis treated with reconstructive surgery and a bone graft and a membrane

PROCEDURE

Treatment with a bone graft

Dental, implants with a diagnosis of peri.implantitis treated with reconstructive surgery and a bone graft alone

Sponsors & Collaborators

  • Kristianstad University

    lead OTHER

Principal Investigators

  • Ann-Marie R Jansåker · Malmö University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-03-01
Primary Completion
2013-01-01
Completion
2013-01-01

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 NCT07678892 on ClinicalTrials.gov