incidence of cesarean in women with spinal and epidural ?analgesia method

Phase 2

Recruiting

• Conditions: Condition 1: painless delivery ?. Condition 2: spinal and epidural anesthesia.; Single spontaneous delivery; Other complications of spinal and epidural anaesthesia during pregnancy

• Registration Number: IRCT2017050920258N46
• Lead Sponsor: Vice chancellor for research, Arak 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: 126

Inclusion Criteria

pregnant women undergoing labor analgesia referred to Taleghani Hospital in Arak; prime gravid; ASA I and II; gestational age 37-42 week; singleton pregnancy
Exclusion criteria: sensitivity to local drugs and narcotics; failure in painless childbirth; ASA class III and IV; patients with mental disorders such as depression, anxiety; patients with gastrointestinal disorders; patients with sleep disorders related to premenstrual syndrome; any use of tranquilizers and sleeping pills

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dilatation in cervix ?. Timepoint: before delivery every 2 hours. Method of measurement: clinical examination.;Uterus contraction ?. Timepoint: before delivery every 1 hours. Method of measurement: clinical observation.;Incidence cesarean ?. Timepoint: after delivery. Method of measurement: count.;Apgar?. Timepoint: one and fifth minute after delivery. Method of measurement: Apgar scale.;Arterial blood gas ?. Timepoint: after delivery. Method of measurement: blood test.