abor pain relief with Entonox

Phase 2

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

• Registration Number: IRCT2017012323559N8
• Lead Sponsor: Vice chancellor for research, Ardabil University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

Over 37 weeks pregnancy, first or second pregnancy, singleton. Exclusion criteria: Malpresentation of fetus? Macrosomia.

Exclusion Criteria

Not provided

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.