Platelet-Rich Plasma for Bone Fracture Treatment: A Systematic Review of Current Evidence in Preclinical and Clinical Studies.
Yangming Zhang, Fei Xing, Rong Luo...
https://pubmed.ncbi.nlm.nih.gov/34414200/Actively Recruiting
Led by Xijing Hospital · Updated on 2026-07-30
300
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the safety and effectiveness of platelet-rich plasma PRP injection therapy to treat knee osteoarthritis and injuries to the surrounding soft tissues. This single-center exploratory study aims to provide a more reliable basis for treating joint injuries by comparing PRP injections to sodium hyaluronate injections. Participants receive injections either with PRP or with sodium hyaluronate into the joint cavity. The study includes different postoperative time points at 6 weeks and 3 months for treatment assessments. Imaging tests such as X-rays, CT scans, and MRI are performed before treatment, 3 weeks after, and 6 months after treatment to monitor changes. During the study, participants undergo comprehensive clinical and imaging examinations to evaluate their joint condition. Researchers collect imaging data at multiple time points to measure treatment effects. The study requires informed consent and monitors participants for safety and effectiveness throughout the treatment and follow-up periods, which continue up to 6 months post-treatment.
CONDITIONS
Effect of Platelet-rich Plasma (PRP) Injection on Knee Osteoarthritis
Y
Yanyan Jia
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Xijing Hospital
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening visit
Duration - Up to 3 months
Participants receive injections of either platelet-rich plasma (PRP) or sodium hyaluronate into the knee joint.
Visits at pre-operation, 3 weeks after treatment, and 6 months after treatment for imaging tests
Duration - Up to 6 months after treatment
Researchers monitor participants through imaging tests to assess joint repair and treatment effects.
Imaging visits at 3 weeks and 6 months post-treatment
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Yangming Zhang, Fei Xing, Rong Luo...
https://pubmed.ncbi.nlm.nih.gov/34414200/Giselle Ramos-Gonzalez, Lianeth Salazar, Olga Wittig...
https://pubmed.ncbi.nlm.nih.gov/36326886/Xijing Hospital
Lead Sponsor