Study comparing two methods of intervention for pain control following total knee replacement
Phase 1
Completed
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecifiedHealth Condition 2: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2018/08/015386
- Lead Sponsor
- Sunshine Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
Patients undergoing Unilateral Primary Total Knee Replacement at Sunshine Hospitals, Secunderabad
Exclusion Criteria
Revision Knee Replacements, Bilateral/Staggered Knee Replacement, Creatinine >2, Infected Cases, Gross Deformity (varus >20 degrees, Fixed Flexion Deformity >15 degrees)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PAIN RELIEF AS MEASURED BY VAS SCORETimepoint: every 8th hourly following surgery for 48 hours
- Secondary Outcome Measures
Name Time Method RANGE OF MOTION AS MEASURED BY GONIOMETERTimepoint: 24 HORS POST SURGERY