Prosperity of celecoxib for pain relief after elective cesarean section delivery, a double-blind randomized controlled trial
Phase 3
- Conditions
- /A
- Registration Number
- TCTR20190109003
- Lead Sponsor
- /A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
-term prgnancy
-singleton
-age 20 †40 year-old
-elective cesarean section or cesarean section with tubal sterilization
-Pfannenstiel incision
-spinal block
-BMI < 35 kg/mm2
Exclusion Criteria
No history of NSAIDs,sulfa group and opioid groug allery
No liver,hematology,renal and heart disease
No currently warfarin tak
Opertive time <= 2 hours
Blood loss<= 1000 ml
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score at rest and movement 24 hour Visual analogue scale,Pain score at rest and movement 6 and 12 hours Visual analogue scale
- Secondary Outcome Measures
Name Time Method PCA pethidine used 24 hours milligram,Pain score at rest and movement 6 and 12 hours visual analogue scale