To evaluate and compare the efficacy and adverse effects of combination levobupivacaine heavy with morphine versus bupivacaine heavy with morphine in lscs under Spinal anaesthesia
Phase 1
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/06/069543
- Lead Sponsor
- JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Parturients of ASA II aged 20 to 40 years with gestational age between 37-42 weeks planned foe elective caesaren section
Exclusion Criteria
Patient refusal
Multiple pregnancy
BMI >30
Patienta with known history of PIH and GDM
Any contraindications to spinal anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess and compare the time taken by the drugs to achieve maximum sensory level and motor blockadeTimepoint: From the commencement of sensory and motor blockade till post operative regression of motor and sensory.
- Secondary Outcome Measures
Name Time Method a) To assess the hemodynamic parameters. <br/ ><br>b) To evaluate postoperative pain. <br/ ><br>c)To monitor for any side effects. <br/ ><br>Timepoint: From the commencement of spinal anaesthesia till post operative recovery period