Osteoarthritis Clinical Trial
Official title:
The Effects of Intraarticular Injection of Platelet-rich Plasma in Patients With Osteoarthritis of the Knee (in a Clinical Trial Phase III)
| Verified date | September 2012 |
| Source | Royan Institute |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Iran: Ethics CommitteeIran: Ministry of Health |
| Study type | Interventional |
Osteoarthritis is the most common type of arthritis. The prevalence of osteoarthritis of the
knee has significantly elevated in the elderly population and youth due to age and sport
activities respectively. Our aims to treat the knee osteoarthritis are including; reduce
knee pain and improve its function; return patients to normal daily activities and reduce
health care costs.
The current treatments which are already being used for osteoarthritis of the knee patients
include:
1. Symptomatic therapy: conservative therapies, physiotherapy, analgesics and
non-steroidal anti-inflammatory drugs.
2. Intra-articular injections of corticosteroids and hyaluronic acid.
3. Current Surgical Therapy: knee arthroplasty, osteotomy, arthrodesis and debridement.
As the low mitotic activity and lack of blood supply cause little ability for the articular
cartilage to repair itself, so injection of platelet-rich plasma (PRP) has recently received
much more attention due to its capacity to do self-healing in treatment of osteoarthritis of
the knee.
PRP consists of several concentrated growth factors in platelets of autologous blood that
are applied to the different parts of medicine such as reconstruction of damaged tissue.
Although platelets are well-known to involve in the blood clots formation, but current
studies have shown that they secrete many bio-proteins which attract macrophages,
mesenchymal stem cells and osteoblasts to remove necrotic tissue in addition to participate
in healing procedure.
This study is a prospective, randomized, controlled trial to assess The positive effects of
platelet-rich plasma injection in 244 patients with osteoarthritis of the knee
| Status | Completed |
| Enrollment | 150 |
| Est. completion date | April 2014 |
| Est. primary completion date | March 2014 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: 1. Age 18 to 65 years 2. Body mass index (BMI) =33 kg/m2 3. Grade 2And above imaging of osteoarthritis 4. History of knee pain or swelling should have at least 4 months Exclusion Criteria: 1. treated with steroids and Anti-coagulant or anti-platelet aggregation 2. history of infectious, systemic diseases, Immune deficiency and coagulation disorders 3. Patients with Hb =11, Plt = 150000 4. Varus > 10 , valgus > 10 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Iran, Islamic Republic of | Royan Institute | Tehran |
| Lead Sponsor | Collaborator |
|---|---|
| Royan Institute |
Iran, Islamic Republic of,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | pain | pain reduction by VAS scoring before injection of PRP and 3,6 and 12 months after last injection | 3 months | Yes |
| Primary | physical activity | physical activity of patients which is measured by WOMAC scoring , before injection of PRP& 3,6 and 12 months after last injection. | 3months | Yes |
| Primary | cartilage repair | The repair of knee cartilage that is evaluated by MRI,before and 12months after injection. | 12months | Yes |
| Secondary | quality of life | Evaluation the quality of life that is measured by SF36,before,3,6 and 12months after injection. | 3months | Yes |
| Secondary | joint replacement | Evaluation the need for joint replacement 12months after injection. | 12months | Yes |
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