Comparison of ropivacaine and bupivacaine for spinal anaesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2022/10/046717
- Lead Sponsor
- Bhabha Atomic Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Patients aged 18-60 years, ASA grade I-II undergoing elective infra-umbilical surgeries, less than 2hours, under spinal anaesthesia.
Exclusion Criteria
Patient refusal
Pregnancy
Allergy to local anesthetic drugs
Any other contra indications to spinal anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study duration of action of hyperbaric ropivacaine and hyperbaric bupivacaine.Timepoint: 24hours
- Secondary Outcome Measures
Name Time Method To study <br/ ><br>1.Time taken to achieve maximum sensory blockade. <br/ ><br>2.Time taken to achieve maximum motor blockade. <br/ ><br>3.Intra-operative hemodynamics. <br/ ><br>4.Time taken for 5 segment regression of sensory block. <br/ ><br>5.Time taken for regression of motor blockade to modified Bromage 1. <br/ ><br>6.Side effects if any <br/ ><br>Timepoint: 24hours