A comparative study between hyperbaric ropivacaine and isobaric ropivacaine foe spinal anesthesia
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/11/060226
- Lead Sponsor
- Dr Sunil Chiruvella
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 & 2
Exclusion Criteria
Patient refusal
Allergic to local anaesthetics
Pregnancy
Absolute contraindications for Regional anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective is to compare onset and duration of sensory and motor blockadeTimepoint: 5 mins <br/ ><br>10 mins <br/ ><br>15 mins <br/ ><br>30 mins <br/ ><br>1 hour <br/ ><br>2 hours <br/ ><br>6 hours <br/ ><br>12 hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary objective is to compare hemodynamic changes, intraoperative analgesia requirement and adverse effects in both groupsTimepoint: 5 mins <br/ ><br>10 mins <br/ ><br>15 mins <br/ ><br>30 mins <br/ ><br>1 hour <br/ ><br>2 hours <br/ ><br>6 hours <br/ ><br>12 hours <br/ ><br>