spinal anaesthesia with , hyperbaric bupivacaine vesrsus ropivacaine
Not Applicable
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/049861
- Lead Sponsor
- Jitendra kalbande
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age 18- 60 years ,ASA 1 and 2 both male and female, duration of surgery - minimum 1 hr
Exclusion Criteria
Patients with contraindication to spinal anaesthesia, allergy to drug being used, patient with neurological deficit, pregnancy women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of onset of sensory block, time taken to achieve T10 segment sensory block, maximum height of block, time to 2 segment regression and complete sensory recovery. Onset of motor block, time taken to achieve complete motor block, complete motor recoveryTimepoint: 0, 2, 4, 6, 8, 10, 12, 14, 20, 25, 30, 40, 50, 60, 90, 120 min, time till requirement of rescue analgesia
- Secondary Outcome Measures
Name Time Method Heart rate, non invasive blood pressure, peripheral oxygen saturation , any adverse effectsTimepoint: 0, 2, 4, 6, 8, 10, 12, 14, 20, 25, 30, 40, 50, 60, 90, 120 min, time till patients shifted to ward from postoperative unit.