The purpose of this study is to evaluate the affect that platelet rich plasma has on the molecular an cellular functioning of the knee joint.
In this study 18 subjects with mild to moderate symptomatic knee osteoarthritis will be recruited per an IRB approved protocol with explicit inclusion and exclusion criteria. Subjects who are enrolled and meet all criteria will be blinded and randomized (2:1) to receive Platelet Rich Plasma or normal saline "control". Prior to the intervention, a synovial fluid aspiration will occur. At follow up number one (approximately 10 days from baseline) a repeat aspiration will occur and a differential analysis of the molecular and biochemical effects will be undertaken; this data will serve as the primary outcome measures. This data will be correlated to clinical and imaging outcome measures which will be secondary outcome measures completed at baseline and intermittently throughout the study. The duration of the study is one year.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
18
Platelet rich plasma injection into knee versus placebo (saline) injection.
Platelet rich plasma injection into knee versus placebo (saline) injection.
Hunter Holmes McGuire VA Medical Center
Richmond, Virginia, United States
Biochemical Molecular Outcomes
Evaluate for change in biochemical molecular milieu temporal response after PRP injection or normal saline (control) compared to baseline, as measured by multiplex suspension array technology.
Time frame: Baseline and 10 day follow up
Clinical Outcomes
Evaluation for change in pain level via VAS and WOMAC at baseline and follow up.
Time frame: 1 year
Imaging Outcomes
Evaluation for change in joint space width using knee radiographs at baseline and 6 month follow up.
Time frame: 6 months
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