Comparison of pain management techniques in cases of Total Knee Replacement surgeries
Not Applicable
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2019/05/018988
- Lead Sponsor
- AFMC Pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age upto 80 yrs, American society of anaesthesiologists grade I to III, Body mass index 18-30 kg/m2
Exclusion Criteria
Patients with comorbidities (morbid obesity, muscular dystrophy, history of stroke or major neurological deficit, sensory and motor disorders etc.., allergic to LAs and opioids, chronic pain requiring opioid medication, bilateral total knee replacement
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for rescue analgesic, total amount of analgesic required keeping the patient pain free during 48 hours of postoperative period, NRS scoreTimepoint: 1 yr
- Secondary Outcome Measures
Name Time Method Total amount of analgesic required keeping the patient pain free during 48 hours of postoperative period, NRS scoreTimepoint: 1 yr