Analgesic effect in normal delivery and Apgar

Not Applicable

• Conditions: Delivery.; O75 Other complications of labour and delivery, not elsewhere classified; XV Pregnan

• Registration Number: IRCT2016040316148N3
• Lead Sponsor: Vice chancellor for research, Sabzevar 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: 120

Inclusion Criteria

Maternal candidate for the Analgesic method using Entonox or spinal for labor

Exclusion criteria : Having contraindicated in the spinal include: the reluctance of patients? infection at the needle insertion? Having coagulation disorders? Increased cranial pressure? contraindicated for use Entonox

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before the intervention After the intervention. Method of measurement: Numerical Pain Scale.;Apgar score. Timepoint: Immediately after birth. Method of measurement: Using Apgar number.;Duration of delivery. Timepoint: The first phase by the end of the fourth phase labor. Method of measurement: With long of time.;Maternal outcomes. Timepoint: Method of use Of Entonox during the use of gas,   In the way of spinal analgesia after spinal half an hour, 12 hours after delivery and before discharge mother. Method of measurement: Using questionnaires.