Assessment of health around implants in patients rehabilitated with Removable or Fixed Prostheses on Implants

Not Applicable

Recruiting

• Conditions: Mucositis, Peri-Implantitis, Dental Implantation; C06.405.205.798; C07.465.693; E04.545.550.280

• Registration Number: RBR-39mpct
• Lead Sponsor: Hospital Universitário Onofre Lopes

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-01-04
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Bimaxillary edentulous; use of double dentures for at least one year; rehabilitation with conventional denture bimaxillary in UFRN; sufficient bone height for implant placement of at least 9,00mm in the mandibular arch.

Exclusion Criteria

Diabetes; smoking; osteoporosis; immune deficiency or anticoagulant therapy; patients with neurological diseases.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Increased mucositis rate in the test group compared to the control group after 01 years and 05 years of evaluation, verified through the evaluation of peri-implant sites with millimeter periodontal probe, from a finding of a variation of at least 20% in pre- and post-intervention measurements.;Increased mucositis rate in the test group compared to the control group after 01 years, verified by the evaluation of peri-implant sites with millimeter periodontal probe, based on the statement of a variation of at least 20% in pre measurements and post intervention.

Secondary Outcome Measures

Name	Time	Method
Absence of periimplantitis in the test and control groups after 05 years of assessment, verified by evaluation of peri-implant sites with periodontal millimeter probe and periapical radiographs, from the observation of increased bone loss than three millimeters in pre and post intervention measurements.;Loss of implants in patients of test and control groups after 01 years of assessment, verified by periapical radiographs, from the observation of non-osseointegration of the implant measurements in pre and post intervention.