A comparison of spinal and epidural analgesia for labor pain and maternal and neonatal outcomes

Phase 2

Recruiting

• Conditions: abor analgesia.; ?Delivery; O80-O84

• Registration Number: IRCT2015053022473N1
• Lead Sponsor: Vice chancellor for research Mashhad 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: Recruiting
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

single or twin term pregnancy, primi and multiparity, cephalic presentation, not use of narcotic drugs, no history of bleeding disorders, normal platelet and INR, no fetal distress, and mother's request for regional labor analgesia.
Exclusion criteria: the mother's unwillingness to continue the study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
abor analgesia. Timepoint: every 15 min. Method of measurement: by visual analogue scale.

Secondary Outcome Measures

Name	Time	Method
eed to resucitation. Timepoint: after birth. Method of measurement: Neonate's respiratory and cardiac status.;Motor block. Timepoint: every 15 min. Method of measurement: Bramage scale.;Duration of delivery. Timepoint: after birth. Method of measurement: based on time (min).;Duration of second stage of labor. Timepoint: after birth. Method of measurement: based on time (min).;Neonate's Apgar score. Timepoint: after birth. Method of measurement: Apgar score.