Determination of adequacy of analgesia in vaginal delivery with persistent intravenous analgesia with remifentanil compared to epidural analgesia

Phase 3

• Conditions: Pain.; F45.4; Pain disorders related to psychological factors

• Registration Number: IRCT20190325043107N14
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 65

Inclusion Criteria

Perform vaginal delivery

Exclusion Criteria

Women candidates for cesarean section

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Every hour for two days. Method of measurement: Visual Analogue Scale.