TCTR20140909001
Not yet recruiting
未知
The study aims to investigate the effectiveness of parecoxib 40 mg in controlling pain after elective cesarean delivery. The subjects were divided into 2 groups: intervention and control group. The intervention includes pregnant women who age over 20
Faculty of Medicine. Siriraj Hospital. Mahidol University0 sites82 target enrollmentSeptember 9, 2014
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Postpartum womenElective cesarean delivery
- Sponsor
- Faculty of Medicine. Siriraj Hospital. Mahidol University
- Enrollment
- 82
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Pregnant women age over 20 years old
- •Admission of elective cesarean delivery
- •Anesthetic method is spinal anesthesia
Exclusion Criteria
- •Contraindication to NSAIDs
- •Allergy to NSAIDs
- •Current medication is warfarin and antifungal drugs
Outcomes
Primary Outcomes
Not specified
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