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

• Conditions: cesarean delivery; Postpartum womenElective cesarean delivery; Parecoxib

• Registration Number: TCTR20140909001
• Lead Sponsor: Faculty of Medicine. Siriraj Hospital. Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2014-09-06
• Study Start: 2014-09-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: Female
• Target Recruitment: 82

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
morphine and its derivatives 24 hours after intervention cumulative doses in mg

Secondary Outcome Measures

Name	Time	Method
pain 24 hours after intervention numeric pain score,Cost 24 hours after intervention total cost of pain control