A clinical trial to compare the efficacy of fentanyl versus magnesium sulphate as adjuvants with 0.75% hyperbaric ropivacaine in spinal anaesthesia for lower abdominal surgeries
Phase 4
Completed
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2024/04/066058
- Lead Sponsor
- Dayanand Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. American Society of Anaesthesiologists physical status grade I & II
2. Age 18 years and above
3. Either gender
Exclusion Criteria
1. Patient not giving consent for spinal anaesthesia
2. Patients who are allergic to the drugs being used
3. Patients in whom spinal anaesthesia is contraindicated
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset and duration of motor and sensory blockTimepoint: Onset and duration of motor and sensory block
- Secondary Outcome Measures
Name Time Method hedodynamics <br/ ><br>efficacy of the drugsTimepoint: intraoperative baseline, every minute for 5 minutes & then every 15 minutes for 90 minutes. Postoperatively every hour for 6 hours