Comparing the efficacy of peripheral nerve blocks and injections within the knee for pain management following Total Knee Replacement
Phase 2
Completed
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2019/11/021861
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
All patients undergoing unilateral Total Knee Arthoplasty for primary osteoarthritis of the knee
Exclusion Criteria
Patients undergoing bilateral surgery
Patients undergoing unicondylar knee arthoplasty
Patients undergoing Totalkneearthoplasty for inflammatory aetiology
Patients with bleeding diathesis
Patients with renalfailure/elevated renal parameters
Patients with pre-existing neuropathies
Patients who have undergone any prior surgery to the affected limb
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analog Scale of more than 6Timepoint: Visual Analog Scale of more than 6 at 6 hours, 12 hours, 24 hours, 48 hours post opeatively
- Secondary Outcome Measures
Name Time Method Knee range of movement post operativelyTimepoint: At 48 hours post operatively