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Clinical Trials/NCT05683405
NCT05683405
Recruiting
N/A

Management of Peri-implantitis: Non-surgical Treatment of Peri-implantitis: Mechanical Debridement vs. Air-polishing

Tannhelsetjenestens Kompetansesenter for Nord-Norge1 site in 1 country88 target enrollmentAugust 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peri-Implantitis
Sponsor
Tannhelsetjenestens Kompetansesenter for Nord-Norge
Enrollment
88
Locations
1
Primary Endpoint
Probing depth
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to compare non-surgical treatment by mechanical debridement with air-polishing in peri-implantitis. The main question it aims to answer is:

• Does non-surgical treatment of peri-implantitis with an air-polishing devise (Perioflow® EMS, Nyon Switzerlad) provide a better treatment result than conventional cleaning with mechanical instruments?

Participants will receive non-surgical treatment of peri-implantitis either with mechanical debridement and with an air-polishing devise.

Researchers will compare pocket depth and bleeding/suppuration on probing in implants treated with the two methods to see if either of them is more efficient in treatment of peri-implantitis.

Registry
clinicaltrials.gov
Start Date
August 1, 2023
End Date
December 2028
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Referred to TkNN (Tannhelsetjenestens kompetansesenter for Nord-Norge) for treatment of peri-implantitis
  • Participants should have at least one implants with peri-implantitis according to the diagnostic criteria from the 2017 Chicago Consensus Meeting.

Exclusion Criteria

  • Cemented prosthetic reconstructions, individuals smoking more than 10 cigarettes per day, individuals with diabetes and poor control of blood glucose levels, antibiotic treatment during the past threee months, and implants that are preferably to be extracted due to prognosis or function, are excluded.

Outcomes

Primary Outcomes

Probing depth

Time Frame: 26 weeks

Probing depth 5 millimeters or more

Bleeding on probing

Time Frame: 26 weeks

Bleeding from pocket on pocket depth probing

Suppuration on probing

Time Frame: 26 weeks

Suppuration from pocket on pocket depth probing

Study Sites (1)

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