Effect of nalbuphine versus fentanyl as an adjuvant in epidural anesthesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036643
- Lead Sponsor
- SMS medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Consent for participation in study
2. Patients posted for urological surgeries belonging to ASA grade 1 and 2
3. Weigh 45 to 70 kg
Exclusion Criteria
1.Obese patients , uncontrollable hypertension, uncontrollable diabetes mellitus ,severe CVS malformation,renal or hepatic failure , with the history of neurological surgeries
2 . H/o spinal surgery , spinal deformity or infection at local site
3 . Coagulation defects those on anticoagulants
4 . Allergic to any of concerned drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method time duration after which first rescue analgesia requiredTimepoint: After surgery when VAS score is 4 or more
- Secondary Outcome Measures
Name Time Method To determine the mean VAS score for first 6 hour , 6 to 12 and 12 to 24 hours. <br/ ><br>2.To determine the percentage of cases who develop side effect( if any ) in both the groups.Timepoint: 24 hours