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Study identifier: NCT06358807 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Microfracture With Platelet Rich Plasma Gel Injection for Osteochondral Lesion of the Talus

Condition: Osteochondral Lesion of Talus · Microfractures · Platelet Rich Plasma  ·  Sponsor: Peking University Third Hospital

PhaseNA
Planned participants70
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if combined local injection of platelet rich plasma (PRP) gel adds clinical efficacy to isolated arthroscopic microfracture in treatment of osteochondral lesion of the talus (OLT). The interface integration of the injured area will also be assessed via radiographic follow-up. The main questions it aims to answer are: * Does arthroscopic microfracture combined with PRP gel injection improve ankle function of participants based on American Orthopedic Foot and Ankle Society (AOFAS) Score? * Does arthroscopic microfracture combined with PRP gel injection improve interface integration of the injured cartilage on magnetic resonance imaging (MRI)? Researchers will compare arthroscopic microfracture with concomitant local injection of PRP gel to isolated microfracture to see if intraoperative PRP gel injection adds clinical efficacy to isolated arthroscopic microfracture in treatment of OLT. Participants will: * Undergo either isolated arthroscopic microfracture or microfracture with intraoperative injection of PRP gel * Receive clinical follow-up 3, 6, 12, and 24 months after surgery and answer scales of ankle function assessment * Take MRI preoperatively and 6, 12 and 24 months after surgery

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

Talk to the study team

Qinwei Guo, MD  ·  +86 18601129252  ·  guoqinwei@vip.sina.com

Fengyi Hu, MD  ·  +86 13335511505  ·  hfy1322@pku.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Peking University Third HospitalBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06358807