Evaluation of Surgical Treatment of Disease involving Dental Implants

Not Applicable

Recruiting

• Conditions: Peri-Implantitis; C07.465.714.282

• Registration Number: RBR-9d2hbm
• Lead Sponsor: niversidade Federal do Rio Grande do Norte

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-04-20
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Volunteers of both sexes; age over 18 years; toothless units, partial or total; patients with single or multiple osseointegrated implants rehabilitated with a minimum period of 12 months; patients with at least one implant with the clinical diagnosis of peri-implantitis according to the criteria of Mombelli (1999).

Exclusion Criteria

Volunteers with severe psychosomatic illnesses that prevent good oral hygiene; diagnosis of systemic conditions that make it impossible to undergo a surgical procedure; hallucinogenic or narcotic drug users; history of antibiotic and / or anti-inflammatory therapy 3 months before the initial evaluation visit; carriers of diseases that cause severe impairment of the immune system.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main primary outcome: Decrease in the degree of peri-implant inflammation and the depth of probing, determined by probing at the beginning of the study and at the end of the study.;Expected primary outcome 2: Maintenance of bone level, determined by measuring in millimeters with a ruler on digital periapical radiography at the beginning of the study and at the end of the study.;Expected primary outcome 3: Decrease in visible biofilm, determined by the presence or absence of biofilm on the faces of teeth and prostheses at the beginning of the study and at the end of the study.