Efficacy of a single intravenous venous dose of Parecoxib 40 mg for post-operative pain control after elective cesarean delivery: a double blind randomized controlled trial
Not Applicable
Completed
- Conditions
- Pregnancyprevious cesarean deliveryParecoxibpostoperative painprevious cesarean delivery
- Registration Number
- TCTR20140618001
- Lead Sponsor
- Siriraj Routine to Research Unit
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 82
Inclusion Criteria
1 Term pregnancy aged over 20 years old
2 Previous cesarean delivery
3 Elective cesarean delivery
4 Analgesia planning is spinal block
5 Able to read and write Thai language
Exclusion Criteria
1. Allergy to NSAIDs
2. Contraindication to NSAIDs use
3. Warfarin or azole drugs use
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Morphine and its derivatives 24 hours after cesarean delivery total doses of morphine and its derivatives
- Secondary Outcome Measures
Name Time Method Pain 24 hours after cesarean delivery Pain score,Breast milk 24 hours after cesarean delivery Time interval after surgery to production of breast milk,Cost 24 hours after cesarean delivery total cost of analgesia for pain control