Ropivacaine for pain management in patients who undergo Caesarean sectio

Not Applicable

Completed

• Conditions: Post-operative pain management in patients who undergo cesarean section; Pregnancy and Childbirth; C-section

• Registration Number: ISRCTN15849443
• Lead Sponsor: Mexican Social Security Institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-02-22
• Study Start: 2022-05-24
• Last Update Posted: 6 June 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 81

Inclusion Criteria

1. Women from 18 to 40 years of age
2. Term pregnancy
3. Undergoing programmed or elective cesarean section

Exclusion Criteria

1. Chronic diseases
2. Placental disorders
3. Infections
4. Aallergies to anesthetics
5. Contraindication to regional anesthesia
6. Obstetric emergency
7. History of drug abuse
8. Inability to understand the visual analog scale

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain was measured using the VAS scale at the end of the surgery (baseline), 2, 6, 12, 18 and 24 hours after surgery.

Secondary Outcome Measures

Name	Time	Method
<br> 1.Use of rescue doses was measured using the VAS scale at the end of the surgery (baseline), 2, 6, 12, 18 and 24 hours after surgery.<br> 2. Days of hospital stay were measured using the medical record over a 10 day period after the surgery<br> 3. Presence of adverse events was measured using medical examination over a 10 day period after the surgery<br>