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Clinical Trials/NCT04259840
NCT04259840
Terminated
Not Applicable

Clinical Outcomes of Resective Surgical Treatment of Peri-Implantitis With or Without Implantoplasty. A Retrospective Study

University of Michigan1 site in 1 country41 target enrollmentDecember 5, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Peri-Implantitis
Sponsor
University of Michigan
Enrollment
41
Locations
1
Primary Endpoint
Therapeutic resolution of the peri-implantitis as measured by radiographic bone loss
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

The aims of the current study are 1) to assess the therapeutic resolution of the peri-implantitis after resective surgical treatment with or without implantoplasty procedure (no further radiographic bone loss, no erythema of the peri-implant mucosa, PD <6mm), and 2) to evaluate the survival rate of the peri-implantitis treated dental implants.

Detailed Description

The records of patients who underwent resective surgical treatment for peri-implantitis at the University of Michigan Graduate Periodontics clinic will be examined and analyzed. Patients who meet the inclusion/exclusion criteria will be contacted and invited to participate in the study to measure the following in a single visit: bleeding on probing, edema, redness of the peri-implant mucosa, and peri-implant probing pocket depth. Additionally, patients will be asked to complete a survey during their study visit regarding their implant(s) and previous peri-implantitis.

Registry
clinicaltrials.gov
Start Date
December 5, 2019
End Date
July 1, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hom-Lay Wang, DDS, MSD, Ph D

Collegiate Professor of Periodontics and Professor of Dentistry

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Therapeutic resolution of the peri-implantitis as measured by radiographic bone loss

Time Frame: Up to 30 years after the implant was treated for peri-implantitis

The implant has no further radiographic bone loss when compared to previous radiographs.

Therapeutic resolution of the peri-implantitis as measured by erythema

Time Frame: Up to 30 years after the implant was treated for peri-implantitis

The implant has no current erythema of the peri-implant mucosa.

Therapeutic resolution of the peri-implantitis as measured by probing depths

Time Frame: Up to 30 years after the implant was treated for peri-implantitis

The implant has probing depths less than or equal to 5 millimeters.

Survival rate of the peri-implantitis treated dental implants

Time Frame: Up to 30 years after the implant was treated for peri-implantitis

Survival rate will be determined by the duration of implant survival (functioning, non-symptomatic implant after peri-implantitis treatment).

Study Sites (1)

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