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

NCT ID: NCT05683405

Last Updated: 2023-06-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

88 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-08-01

Study Completion Date

2028-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Peri-Implantitis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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

TREATMENT

Blinding Strategy

SINGLE

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

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Mechanical debridement

Group Type EXPERIMENTAL

Non-surgical treatment of peri-implantitis with mechanical debridement

Intervention Type PROCEDURE

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

Air polishing

Group Type EXPERIMENTAL

Non-surgical treatment of peri-implantitis with air polishing

Intervention Type PROCEDURE

Non-surgical treatment of peri-implantitis with air polishing

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Non-surgical treatment of peri-implantitis with mechanical debridement

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

Intervention Type PROCEDURE

Non-surgical treatment of peri-implantitis with air polishing

Non-surgical treatment of peri-implantitis with air polishing

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Malmö University

OTHER

Sponsor Role collaborator

Tannhelsetjenestens Kompetansesenter for Nord-Norge

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Tannhelsetjenestens kompetansesenter for Nord-Norge

Tromsø, Troms, Norway

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Norway

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Elin Hadler-Olsen, PhD

Role: CONTACT

+47 48 06 72 49

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Elin Hadler-Olsen

Role: primary

+4748067249

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

343997

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

SPiT-frequency II_Peri-implantitis
NCT06737315 NOT_YET_RECRUITING NA
Surgical Treatment of Peri-implantitis Defects
NCT06614426 NOT_YET_RECRUITING NA