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Comparison of the Effectiveness of Two Different Surgical Therapeutic Protocols of Peri-implantitis

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. 3 versions Re-verified since Dec 28, 2024, no change to tracked fieldsv5-v7
  2. Primary and study completion dates: Dec 2024 to Dec 2026v4
  3. Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Start date changed from estimate of Jul 2023 to Jul 28, 2023v3 Show 2 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Jul 2023 to Jul 28, 2023
  4. Primary endpoints revised (4) Start date: Jun 2023 to Jul 2023 · Secondary endpoints: 33 to 35 · Eligibility criteria expanded, about 4 wordsv2 Show 3 more changesShow less
    • Start date: Jun 2023 to Jul 2023
    • Secondary endpoints: 33 to 35
    • Eligibility criteria expanded, about 4 words

    See this version in full on ClinicalTrials.gov ↗

  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of the present study is to compare the 1-year clinical, radiographic and microbiological outcomes and patients' satisfaction following surgical treatment of peri-implantitis after applying two different surface modification methods. Secondarily, analysis and comparison of the microbiological results of implants diagnosed and treated for peri-implantitis with healthy implants will be performed.
Trial Details
NCT Number NCT05899933
Lead Sponsor National and Kapodistrian University of Athens
Conditions Peri-Implantitis, Peri-Implant Health
Enrollment 45 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov