A new method of pain relief after caesarean delivery
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indicationHealth Condition 2: O82- Encounter for cesarean delivery without indicationHealth Condition 3: O82- Encounter for cesarean delivery without indicationHealth Condition 4: 1- Obstetrics
- Registration Number
- CTRI/2021/03/032379
- Lead Sponsor
- Dr Hiteshi V
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Women undergoing caesarean section at Gestational age > 34 weeks with American society of Anesthesiologists (ASA) score of I-II
2. BMI -18.5 to 29.5 kg/m2
Exclusion Criteria
1. Pregnant women with known allergy to drug bupivacaine
2. Thrombocytopenia, HELLP Syndrome, Eclampsia, Connective tissue disorders, Anti phospholipid antibody syndrome
3. Women requiring General Anesthesia
4. Local infection at site of injection.
5. Severe maternal or fetal compromise.
6. Prolonged duration of surgery (due to PPH, bladder injury).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method