abor pain relief with remifentanil

Phase 2

• Conditions: abor pain.; Delivery; O80, O84

• Registration Number: IRCT20150808023559N16
• 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: 26 March 2018

Recruitment & Eligibility

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

Inclusion Criteria

Over 37 weeks pregnancy
First or second pregnancy
Singleton

Exclusion Criteria

Malpresentation of fetus
Macrosomia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before analgesic administrations and two times (30 and 60 min) after intervention. Method of measurement: Visual analog scale.

Secondary Outcome Measures

Name	Time	Method
Apgar. Timepoint: 1 and 5 minutes after birth. Method of measurement: Apgar test.