Management of Peri-implantitis: Non-surgical Treatment of Peri-implantitis.

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

Status

Recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05683405

Enrollment

Registered

2023-01-13

Start date

2023-08-01

Completion date

2028-12-31

Last updated

2023-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peri-Implantitis

Keywords

Peri-implantitis, Non-surgical treatment, Air-polishing, Mechanical debridement, Bleeding on probing, periodontal pocket depth

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.

Interventions

PROCEDURENon-surgical treatment of peri-implantitis with mechanical debridement

Non-surgical treatment of peri-implantitis with mechanical debridement .

PROCEDURENon-surgical treatment of peri-implantitis with air polishing

Non-surgical treatment of peri-implantitis with air polishing

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Outcomes Assessor)

Masking description

A periodontist that is not involved in the treatment and who is blinded to the treatment received will evaluate the treatment results.

Intervention model description

Each participant will be randomized to non-surgical treatment of peri-implantitits with either mechanical debridement or with air-polishing.

Eligibility

Sex/Gender

ALL

Age

18 Years to 85 Years

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
Probing depth	26 weeks	Probing depth 5 millimeters or more
Bleeding on probing	26 weeks	Bleeding from pocket on pocket depth probing
Suppuration on probing	26 weeks	Suppuration from pocket on pocket depth probing

Countries

Norway

Contacts

Primary ContactElin Hadler-Olsen, PhD

elin.hadlerolsen@tffk.no+47 48 06 72 49

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026