← Eichor
Study identifier: NCT07550127 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Peri-implantitis Management: Surgical and Maintenance Outcomes

Condition: Peri-implantitis  ·  Sponsor: University of Pittsburgh

PhaseNA
Planned participants44
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn how two standard surgical treatments for peri-implantitis affect inflammation around dental implants. Participants will be randomly assigned to receive resective surgery with implantoplasty or resective surgery with mechanical debridement only. Participants will provide blood samples before surgery, about 48 hours and 2 weeks after surgery. Participants will also provide a small gum tissue sample and fluid from around the implant at baseline and about 3 months after surgery. Participants will be followed in a maintenance program for up to 5 years.

This description comes directly from the study's public registry record.

Talk to the study team

Andrea Ravida, DDS, MS, PhD  ·  7347309678  ·  andrearavida@pitt.edu

Carla Sanchez, MS  ·  4126241179  ·  cab28@pitt.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Pittsburgh School of Dental MedicinePittsburgh, Pennsylvania, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07550127