A comparative study of two doses 15mg versus 30 mg of ketorolac for pain relief in cesarean delivery
Phase 4
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2024/01/061383
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Term gestation,
Age 18-40 years,
ASA physical status I-II,
Cesarean delivery,
Primary or repeat cesarean section,
Pfannenstiel incision
Spinal anesthesia.
Exclusion Criteria
Bleeding disorder,
History of allergy to study drug
History of gastrointestinal ulcer
Conversion to general anesthesia
Obesity (BMI > 35kg/m2)
Preeclampsia
Renal insufficiency
Liver disorder
History of bronchial asthma
Surgical complications
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method