itrous oxide versus pethidine for reducing labor pain in primi -gravid women in Alavi –hosiptial Ardabil

Not Applicable

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

• Registration Number: IRCT201503244256N6
• 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: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

singleton pregnancy (41-37 weeks); active phase of labor; cephalic presentation; absence of fever or severe systemic disease; lack of fetal distress; lack of meconium; lack of coagulation.
Exclusion criteria: FHR abnormality in fetus; lack of progression and macrosomia; delivery with vacuum or? cesarean.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
abor pain. Timepoint: active phase of labor. Method of measurement: Visual analogue scale.

Secondary Outcome Measures

Name	Time	Method
abor's complications. Timepoint: Delivery. Method of measurement: Visual analogue scale and monitoring.