Comparison of Two Different doses Used in adductor canal Block after Knee surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2019/05/019183
- Lead Sponsor
- no
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Eligible participants will be patients scheduled for unilateral, primary TKA with spinal anesthesia, age 48 years old or older, with an American Society of Anesthesiologists physical status classification of Iâ??III, and with the ability to perform the timed up and go (TUG) test preoperatively.
Exclusion Criteria
Exclusion criteria include body mass index exceeding 40 kg/m2 , daily intake of â??strongâ?? opioids (e.g., morphine, fentanyl) during the last 4 weeks, allergy to the medicines used in the study, rheumatoid arthritis, neuromuscular pathology in the lower limbs, pregnancy, inability to cooperate, non-Hindi speakers, and alcohol and/or drug abuse
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total postoperative <br/ ><br>Fentanyl consumption over 24 hour.Timepoint: 24 hour.
- Secondary Outcome Measures
Name Time Method <br/ ><br>Secondary outcomes are <br/ ><br>visual analog scale pain scores rest at various time interval <br/ ><br>Quadriceps femoris strength on PODs 1 and 2, <br/ ><br>Timepoint: 3 months