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Effect of Platelet-rich Plasma (PRP) Injection on Knee Osteoarthritis

Therapeutic Effect of Platelet-rich Plasma (PRP) Injection on Knee Osteoarthritis and Periarticular Tissue Injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06082531
Enrollment
300
Registered
2023-10-13
Start date
2023-09-01
Completion date
2026-12-31
Last updated
2026-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Platelets-rich Plasma, Osteoarthritis Knees Both, Meniscus Disorder, Cartilage Injury

Keywords

platelets-rich plasma, Osteoarthritis, Cartilage Injury, Meniscus Injury

Brief summary

To evaluate the safety and effectiveness of PRP injection therapy in the repair of osteoarthritis and periarticular soft tissue injury through a single-center, exploratory clinical study, and to provide a more reliable basis for the treatment of joint injury.

Interventions

The control group was injected into the joint cavity with sodium hyaluronate injection..

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* The age range of the participants was 20 to 60 years old. Through a comprehensive clinical and imaging examination, it was conclusively determined that the individuals had knee osteoarthritis or experienced injuries to the cart, and meniscus surrounding the knee joint. * The preoperative routine tests and examinations revealed no contraindications. * Revised sentence: "Informed consent of the patient

Exclusion criteria

* The platelet count or function exhibits significant abnormalities、Systemic infection transmitted through the bloodstream. * Prolonged usage of anti-inflammatory drugs and systemic corticoid administration. * In injection site or damage to the skin. * Patients with tumors or undergoing radiotherapy and chemotherapy. * Pregnant or breastfeeding women. * Individuals with mental illnesses who are unable to cooperate with follow-up procedures. * Contraindications for MRI、Patients or their families do consent to participate in the study. * Other circumstances that render participation in the study unsuitable.

Design outcomes

Primary

MeasureTime frameDescription
X-raypre-operation,3 weeks after treatment, 6 months after treatmentThe postoperative plain X-ray film was utilized for the assessment of knee joint deformity, stenosis of the joint space, and hyperplasia of osteophytes.
CTpre-operation,3 weeks after treatment, 6 months after treatmentThe application of three-dimensional CT scan for the assessment of articular cartilage defects.
MRIpre-operation,3 weeks after treatment, 6 months after treatmentThe injury of ligaments, meniscus, and the knee joint was assessed using MRI.

Countries

China

Contacts

CONTACTYanyan Jia
xiyyllwyh@163.com+862984771794

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026