A study to compare the effects of 0.5% hyperbaric bupivacaine and 0.5% hyperbaric levobupivacaine for spinal anaesthesia in cesarean sectio
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2023/03/050810
- Lead Sponsor
- Dr Ashwini Buragohain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA physical status 2
2. Normal singleton pregnancy with a gestational period of minimum 37 weeks
3. Elective cesarean section under spinal anesthesia
4. Informed and written consent.
5. Normal BMI range (18.5-24.9)
Exclusion Criteria
1. Allergy to study drugs
2. Infection at the site of block
3. Patient with known coagulopathy or patients on anticoagulation therapy.
4. Patient with pregnancy induced hypertension or gestational diabetes mellitus
5. Patient with fetal distress
6. Patient with cardiac and renal disease
7. Any neurological deficit in lower limbs, spinal deformity, previous spinal surgery if any
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia in each groupTimepoint: Time from injection of drug administration to the patients first request for rescue analgesia or NRS score more than 4
- Secondary Outcome Measures
Name Time Method To compare the duration of analgesia in each groupTimepoint: Time from injection of drug administration to the patients first request for rescue