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Clinical Trial Summary

The purpose of this single-center, double-blinded randomized control trial with prospective data collection is to assess the ability of platelet rich plasma (PRP) treatment to reduce the level of pro-inflammatory synovial fluid biomarkers following an acute anterior cruciate ligament (ACL) tear. The study will collect and analyze synovial fluid of patients presenting with an acute anterior cruciate ligament (ACL) tear with a second synovial fluid sampling at the time of surgery. It will compare synovial fluid biomarker levels between those receiving an intra-articular Platelet Rich Plasma (PRP) injection versus an intra-articular saline injection serving as a control. Post-operative clinical outcomes will also be assessed, including post-operative pain levels, incidence of post-operative knee stiffness and patient reported outcome scores.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • ACL - Anterior Cruciate Ligament Rupture
  • ACL Injury
  • Anterior Cruciate Ligament Injuries
  • Rupture

NCT number NCT03389685
Study type Interventional
Source NYU Langone Health
Contact
Status Withdrawn
Phase Phase 2
Start date September 9, 2018
Completion date February 2024

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