An evaluation of a low-cost platelet-rich plasma for osteoarthritis of the knee: A pilot study.
Daniel M Cushman, Luke A Johnson, Taylor Burnham...
https://pubmed.ncbi.nlm.nih.gov/40919485Actively Recruiting
Led by University of Utah · Updated on 2026-05-06
10000
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the use of Platelet-Rich Plasma (PRP) injections for treating various musculoskeletal (MSK) conditions, including osteoarthritis (OA) in multiple joints, tendinopathies, and plantar fasciitis. The study aims to track changes in pain, function, and patient satisfaction over a one-year period after receiving PRP, helping to build a detailed registry of treated patients. PRP has gained attention as a treatment with potential benefits and lower risks compared to corticosteroids, which are commonly used for these conditions. Participants who qualify and agree to join will receive a PRP injection prepared from their own blood. This involves drawing blood, spinning it in a centrifuge to concentrate platelets in the plasma, and then injecting this platelet-rich plasma into the affected area. The process keeps the blood sealed from air and uses specialized equipment for preparation. Follow-up surveys will be completed at multiple points: 2 weeks, 6 weeks, 3 months, 6 months, and 12 months after the injection. During the study, participants will undergo blood analysis to evaluate the PRP composition and complete various assessments measuring pain, function, and satisfaction. Outcome measures include the Visual Analog Score for pain, global satisfaction, and condition-specific tools such as the Western Ontario and McMaster Universities Arthritis Index for knees and other joint outcome questionnaires. The study will monitor these measures over 12 months, with a primary focus on pain at 6 months, to assess the effects of PRP treatment on MSK conditions.
CONDITIONS
Platelet Rich Plasma for Musculoskeletal Conditions
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single treatment visit
Participants receive a Platelet-Rich Plasma (PRP) injection prepared from their own blood to treat their musculoskeletal condition.
1 visit (in-person) for blood collection and PRP injection
Duration - 12 months
Participants complete follow-up surveys to assess pain, function, and satisfaction after the PRP injection.
Surveys at 2 weeks, 6 weeks, 3 months, 6 months, and 12 months (remote or in-person)
Total: 1 location
1
University of Utah Orthoaedic Center
Salt Lake City, Utah, United States, 84111-1334
Actively Recruiting
C
Christina Geisler, MS
J
Jamie Egbert, MS
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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