Osteoarthritis, Knee Clinical Trial
— MSCPRPOAKOfficial title:
Autologous Bone Marrow Derived Mesenchymal Stem Cells Enhanced With Platelet Rich Plasma Versus Platelet Rich Plasma In Osteoarthritis Knee:A Comparative Study
Osteoarthritis (OA) is one of the most common joint diseases.This disease commonly develops in the weight bearing joints of the lower limbs, such as the knee and hip joints. Osteoarthritis is considered a chronic degenerative disorder that is characterized by a loss of articular cartilage. Pathogenesis can involve all of the major articular tissues including cartilage, synovial membrane, subchondral bone and other connective tissues such as ligaments and tendons3. There is no effective therapy available today that alters the pathobiologic course of the disease.In view of vast role of platelet derived growth factors, mesenchymal cells and its safety, this prospective clinical trial is designed in an attempt to compare the efficacy of mesenchymal stem cells enhanced with platelet rich plasma in early stages of knee osteoarthritis.
| Status | Recruiting |
| Enrollment | 24 |
| Est. completion date | June 2014 |
| Est. primary completion date | June 2014 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 40 Years to 75 Years |
| Eligibility |
Inclusion Criteria: 1. Grade 1 or Grade 2 Osteoarthritis knee as per Ahlbacks radiographic staging 2. Patients willing to give consent Exclusion Criteria: 1. Osteoarthritis secondary to joint inflammatory diseases (eg- rheumatoid arthritis, ankylosing spondylitis etc) 2. Patients with other diseases, affecting the knee joint like crystal arthropathy, symptomatic chondrocalcinosis, acute synovitis, excessive joint effusion(>100ml), cystic disease around the knee joint(eg-popliteal cyst) 3. Advanced stage of osteoarthritis 4. Bone marrow suppression 5. Co morbidities like pregnancy, cancer, immunosuppression, 6. Osteoarthritis secondary to trauma |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| India | Department of Orthopaedics Postgraduate Institute of Medical Education & Research | Chandigarh |
| Lead Sponsor | Collaborator |
|---|---|
| Aditya K Aggarwal | Postgraduate Institute of Medical Education and Research |
India,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Quantitative articular cartilage volume analysis | by MRI of the knee joint. will be obtained on a GE 3.0 T magnet in the sagittal coronal planes using matching excitation times (NEX), repetition times (TR), and echo times (TE). | Participants will be followed upto an average of 6months. | Yes |
| Primary | Pain relief | Pain will be measured using Visual analogue scale (VAS)which consists of markings from 1 to 10. | Participants will be followed upto an average of 6months. | Yes |
| Secondary | Functional Outcome | Functional Outcome will be assessed by Western Ontario and McMaster Universities score(WOMAC)and Knee Injury and Osteoarthritis Outcome Scores(KOOS) at 6weeks, and 6months | Participants will be followed upto an average of 6months. | Yes |
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