The effect of paracetamol and ketorolac with fentanyl pump on post-cesarean pain control

Phase 3

• Conditions: Postoperative pain control cesarean section.; Delivery by emergency caesarean section

• Registration Number: IRCT20190518043628N1
• Lead Sponsor: Ardabil University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

Pregnant women with cesarean indication
Obtaining patient satisfaction

Exclusion Criteria

Previous proven sensitivity to anesthetics

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Pain will be assessed at 2, 6, 12 and 24 hours after cesarean section. Method of measurement: NRS (numerical rating scale) questionnaire.