A randomised study to compare duration of analgesia when fentanyl or butorphanol or normal saline are added to 0.5 % bupivacaine intrathecally for LSCS.
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2020/07/026284
- Lead Sponsor
- Dept of Anaesthesia and Crtitcal Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I and II
hemodynamically stable
Cessarian section
Exclusion Criteria
- Emergency caesarean section.
- Contraindications to regional anesthesia such as local infections/sepsis at the site of lumbar puncture, space occupying lesions of the brain, anatomical disorders of spine, shock, etc
- Hypersensitivity to study drugs
- Deranged coagulation profile INR > 1.5 and a PTT > 40.
- History of opioid dependence
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method