MedTrace Logo

Clinical Outcomes of Resective Surgical Treatment of Peri-Implantitis With or Without Implantoplasty

NCT04259840 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 41

Last updated 2021-01-11

No results posted yet for this study

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.

Conditions

  • Peri-Implantitis

Interventions

OTHER

Observation

Soft tissue implant measurements

Sponsors & Collaborators

Principal Investigators

  • Hom-Lay Wang, DDS MSD PhD · Department of Periodontics and Oral Medicine, University of Michigan

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-05
Primary Completion
2020-03-10
Completion
2020-07-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04259840 on ClinicalTrials.gov