CTRI/2021/08/035737CompletedPhase 3
To assess the effectiveness of Ultrasound guided genicular nerve block using 0.5% Bupivacaine in comparison with Ultrasound guided intra articular injection of 40mg Depo-Medrol in the management of chronic osteoarthritis knee pain-Double blinded randomized controlled trial
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Christian Medical College
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Chronic osteoarthritis knee with more than 3 months of pain with pain scored by visual analog scale more than or equal to 40mm
- •Radiological osteoarthritis grade greater than Kellegren Lawrence grade 2
- •Refractory knee osteoarthritis pain not alleviated with first line of treatment
- •Well controlled diabetes
- •No signs of active infection at injection site
Exclusion Criteria
- •Patients who underwent prior knee surgery or surgery scheduled in the next 3 months
- •Patients with severe knee joint instability
- •Patients with serious neurological or psychiatric illness
- •Those received steroid or hyaluronic acid injection therapy in last 3 months
- •Those who on anticoagulant medication use and those with severe bleeding diathesis
- •Patients with hypersensitivity to local anaesthetics or steroids
Investigators
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