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To compare the efficacy of intraarticular injection of platelet rich plasma with bupivacaine and steroid combination in osteoarthritis knee and to assess improvement in pain score and patient satisfaction.

Comparison of efficacy of intraarticular injection of platelet rich plasma with bupivacaine and steroid combination in osteoarthritis knee.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033331
Enrollment
50
Registered
2021-05-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Intraarticular injection of platelet rich plasma. Group II patients will be administered 6 ml of PRP prepared by collecting 20 ml of patients blood running it through a centrifuge for 1

Sponsors

Pt BD Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Fifty patients of either sex, age more than 50 years, attending Pain Clinic and fulfilling following three criteria will be included in the study: History, physical examination and pain pattern consistent with osteoarthritis of knee X-ray knee joint findings corresponding with the patient’s clinical symptoms Failure to respond to six weeks of conservative treatment.

Exclusion criteria

Exclusion criteria: Patients with History of uncontrolled diabetes mellitus History of immunodeficiency, collagen vascular disorders or autoimmune disorders Infection or active wound in the knee area Recent history of severe trauma to the knee or knee surgery History of treatment with anticoagulants and antiplatelet drugs 10 days before injection History of NSAID use two days before injection History of intra-articular steroid injection in the past three months History of systemic use of steroid two weeks before the injection Hb values History of adverse drug reaction to local anesthetics or steroids

Design outcomes

Primary

MeasureTime frame
Assessment of pain using pain scoreTimepoint: Half hour before procedure Half hour after procedure 2 weeks after procedure 1 month after procedure 2 months after procedure 3 months after procedure

Secondary

MeasureTime frame
The Western Ontario and McMaster Universities (WOMAC) Index of OsteoarthritisTimepoint: The WOMAC Index will be calculated half hour before the procedure; two weeks, one month, two months and three months after the procedure.;Patient satisfaction Timepoint: Patient satisfaction will be assessed two weeks, one month, two months and three months after the procedure.

Countries

India

Contacts

Public ContactDr Aditi

Pt B.D. Sharma ,PGIMS,Rohtak

drnaveenmalhotra@yahoo.co.in9812091051

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026