Comparing Ropivacaine and Levobupivacaine in ultrasound guided Adductor canal nerve block for early mobility in patients undergoing Anterior Cruciate Ligament reconstruction surgery.
Not Applicable
- Conditions
- Health Condition 1: S83- Dislocation and sprain of joints and ligaments of knee
- Registration Number
- CTRI/2021/07/034754
- Lead Sponsor
- Dr RML HOSPITAL AND ABVIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients scheduled to undergo elective ACL reconstruction surgery under general anesthesia.
Exclusion Criteria
Pre-existing coagulation disorders.
Local infection at the site of injection.
Allergy to study drug(prior test dose will be given)
Chronic Pain syndrome
Patients who received any analgesia 24 hours prior to surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-operative quadriceps muscle strength using SLR (straight leg raise) test.Timepoint: Post operatively every 2 hourly till 4 hours and 4 hourly for the next 20 hours
- Secondary Outcome Measures
Name Time Method Time from end of surgery to first rescue analgesia requirement.Timepoint: This will be measured from the time of administration of block to the first instance when VAS score will be equal or more than 4 during the 24 hour period while the the patients will be assessed at 2nd,4th,8th,12th,16th,20th,24th and in between if patient complains of pain.;Total rescue Analgesia in 24 hours.Timepoint: Injection tramadol will be administered intravenously when VAS score is equal or more than four. The total amount of tramadol consumed in 24 hours will be noted.