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RECRUITING
NCT05412381
PHASE3

PRP in ACLR to Prevent PTOA

Sponsor: Hospital for Special Surgery, New York

View on ClinicalTrials.gov

Summary

The purpose of our study is to examine the effect of platelet-rich-plasma (PRP) injection on the short-term resolution of post-injury inflammation (biomarkers) and improvement in joint function in patients with acute ACL injury. This RCT has been powered based on the questionnaire KOOS Jr. but it is considered a 'pilot study' in terms of the lab analysis proposed.

Official title: Platelet Rich Plasma (PRP) Treatment of the Anterior Cruciate Ligament Injured Knee to Decrease the Risk of Post-traumatic Osteoarthritis (PTOA): a Randomized Double-blind Controlled Trial

Key Details

Gender

All

Age Range

14 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

56

Start Date

2022-06-27

Completion Date

2026-12-31

Last Updated

2026-02-13

Healthy Volunteers

No

Interventions

PROCEDURE

platelet rich plasma (PRP) injection

We aim to evaluate early catabolic and inflammatory changes in knee joints in patients receiving PRP injections following ACL injury, as these patients are at higher risk of developing PTOA. We also aim to establish correlations between markers of biologic activity of PRP and clinical outcomes (including both patient-reported outcomes and clinical functional outcomes), with emphasis on cellular and molecular inflammatory parameters modulated by PRP.

PROCEDURE

placebo saline injection

Patients randomized into the control arm will receive the placebo or saline injection

Locations (1)

Hospital for Special Surgery

New York, New York, United States