Comparison of 2 block techniques for post cesarean pain relief.
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2018/12/016494
- Lead Sponsor
- Dr Aman Malawat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patient with ASA Class II, III
2. Normal singleton pregnancy with a gestation of at least 37 weeks
3. Patientâ??s written and informed consent
Exclusion Criteria
1. Patient with ASA Class IV & V
2. Patient refusal
3. Local infection at the site of injection
4. Allergy to study medications
5. Anatomic abnormalities
6. Systemic anticoagulation or coagulopathy
7. Inability to comprehend or participate in pain scoring system
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare time of first rescue analgesic needed.Timepoint: To compare time of first rescue analgesic needed.
- Secondary Outcome Measures
Name Time Method To compare severity of postoperative pain via visual analogue pain scale at rest (VASR) and with movement (dynamic)Timepoint: 48 hours;To compare the total cumulative dose of analgesic needed in first 48 hours after surgery.Timepoint: 48 hours