To compare spinal anesthesia using bupivacaine heavy (0.5%) with fentanyl to ropivacaine heavy (0.75%) with fentanyl in lower segment Cesarean section.
Phase 4
- Conditions
- Health Condition 1: O30-O48- Maternal care related to the fetus and amniotic cavity and possible delivery problemsHealth Condition 2: I95-I99- Other and unspecified disorders of the circulatory systemHealth Condition 3: O94-O9A- Other obstetric conditions, not elsewhere classifiedHealth Condition 4: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2023/09/057213
- Lead Sponsor
- Alok Kumar Bharti
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Full term pregnancy
ASA I and II
LSCS
Exclusion Criteria
patient refusal, having allergy to studied drugs, any contraindication to spinal anaesthesia, multiple pregnancies, suspected fetal abnormality or complicated pregnancies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess Block characteristics objectively.Timepoint: Till sensory motor blockade achieved as per protocol
- Secondary Outcome Measures
Name Time Method To assess hemodynamic parameter postoperative analgesia, time to first rescue side effectsTimepoint: till first rescue analgesia required;To assess hemodynamic parameter, duration of postop analgesia time to first rescue analgesia side effects seenTimepoint: Time to first rescue analgesia needed