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Long-term Surgical Treatment Outcome of Peri-implantitis Lesions

NCT05339789 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 650

Last updated 2024-02-16

No results posted yet for this study

Summary

The surgical treatment outcome of patients that have been or are consecutively treated at the University of Malmö, at Blekinge hospital, and at the Dental Clinic of the Sigmund Freud University Vienna will be evaluated on an a regular base; specifically all patients treated since 2014 and those receiving treatment in the future, will be regularly assessed, max. once per year after the 1-year control from the surgical intervention for clinical and radiographic assessment of healing. Clinical peri-implant parameters (e.g., probing pocket depth) and peri-implant sulcus fluid (PISF) are collected, and a peri-apical radiographic examination is made. Further, from 200 patients treated in the future, the inflammatory peri-implant lesion will be collected and subjected to histological, microbiological, and molecular analysis. The removal of these lesions is a standard procedure and performed in all patients independent of study participation; i.e., the lesion has anyway to be removed during surgery and if the lesions are not stored, they would be thrown.

Conditions

  • Peri-Implantitis

Sponsors & Collaborators

  • Medical University of Vienna

    collaborator OTHER

  • Sigmund Freud PrivatUniversitat

    collaborator OTHER

  • Blekinge County Council Hospital

    collaborator OTHER

  • Malmö University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
130 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-30
Primary Completion
2030-12-31
Completion
2030-12-31

Countries

  • Austria
  • 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 NCT05339789 on ClinicalTrials.gov