To compare the analgesic efficacy of two block techniques for post cesarean patients.
Not Applicable
- Conditions
- Health Condition 1: O759- Complication of labor and delivery, unspecified
- Registration Number
- CTRI/2018/11/016420
- 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
•Patient with ASA Class I, II, III
•Normal singleton pregnancy with a gestation of at least 37 weeks
•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
- Secondary Outcome Measures
Name Time Method