Observational Study of PRP and PRF in TMJ Surgery

This observational study is looking at adults who have had temporomandibular joint (TMJ) surgery. The goal is to see how well two treatments, platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) injections, work when given during surgery. Researchers want to compare if PRP or PRF helps with pain after surgery and how well your jaw recovers. They will also look at how these treatments affect jaw function, like how wide you can open your mouth. You could be eligible if you are between 18 and 75 years old and have already had TMJ arthroscopy with either PRP or PRF.

Study design
This is an observational study with a planned enrollment of 700 participants. It is not a randomized trial, meaning participants are not assigned to a treatment group.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants' pain intensity will be assessed from baseline to 6 months post-surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07359131

Postoperative Assessment of Platelet-Rich Plasma and Platelet-Rich Fibrin in Temporomandibular Joint Surgery

Not Yet Recruiting
Not specifiedAges 18–75Observational
Jingping Wang, MD, Ph.D.
~700 participants
Updated 2026-06-09 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
pain intensity
Measured over from baseline to 6 months post-surgery.
Temporomandibular Joint Disorders
1 sites across 1 states
Massachusetts1

Opens a ready-to-send draft in your own email app — review before sending.

  • pain intensityfrom baseline to 6 months post-surgery.

    The primary endpoint of the study is the change in pain intensity from baseline to 6 months post-surgery.