A DOUBLE BLIND RANDOMIZED CONTROL TRIAL TO COMPARE POSTOPERATIVE ANALGESIA WITH EPIDURAL BUPIVACAINE 0.25% AND ROPIVACAINE 0.2%
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/049743
- Lead Sponsor
- Bharati hospital and Research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)American Society of Anaesthesiologists (ASA) Grade I & II patients,of both sexes.
2)Patients undergoing Lumbar spine surgery under GA
3)Patients in the age group of above 18years
Exclusion Criteria
1)Individuals not willing to participate in the study
2)any previous local anesthetic or opioid allergy
3)a history of previous spine surgery,
4) Individuals with sensory and motor deficits
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO COMPARE EPIDURAL 0.25% BUPIVACAINE AND 0.2% ROPIVACAINE FOR <br/ ><br>POST OPERATIVE ANALGESIA IN SPINE SURGERYTimepoint: post operative 48 hours
- Secondary Outcome Measures
Name Time Method 1)To compare VAS score between two groups. <br/ ><br>2)To compare Bromage scale under the effect of Bupivacaine and Ropivacaine. <br/ ><br>3)To compare the time to perform the specific maneuvers between two groupsTimepoint: post operative 48 hours