A Study of Ropivacaine versus Bupivacaine under Spinal Anaesthesia in Lower Abdominal and Lower Limb Surgeries
Phase 3
- Registration Number
- CTRI/2024/04/065441
- Lead Sponsor
- Department of Anaesthesia MMIMSR
- 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 or II, 18-60 years, either sexes, 50-70 kgs, patients for lower abdominal and lower limb surgeries
Exclusion Criteria
Negative consent, surgery more than 3hrs, drug sensitivity, disease or deformity of spine, infection at puncture site, coagulation disorders, pregnant/lactating, psychiatric patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the onset, duration and level of sensory blockade achieved after intrathecal administration of the two drugs.Timepoint: Intraoperative period after spinal anesthesia
- Secondary Outcome Measures
Name Time Method To compare the characteristics of spinal block and hemodynamic changes among the two study groupsTimepoint: Intraoperative and post operative period after SA