The effect of intrathecal Midazolam in the severity of pain in Cesarean Section: A randomized controlled trial?

Phase 2

• Conditions: Pain in caesarean section.; Delivery by elective caesarean section

• Registration Number: IRCT138807121310N4
• Lead Sponsor: Kermanshah 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: 124

Inclusion Criteria

Inclusion criteria included: No presence of severe spinal lesion, No presence of abscess or infection of skin and soft tissue in the location of needle insertion, No presence of sever anxiety and restlessness, No presence of Central Nervous System lesion, No presence of peripheral nerve lesion, No presence of significant mental disorders or drug abuse, Age 18-45 year.

Exclusion criteria: severe spinal lesion, abscess or infection of skin and soft tissue in the location of needle insertion, sever anxiety and restlessness, Central Nervous System lesion, presence of peripheral nerve lesion, presence of significant mental disorders or drug abuse. Age less than 18 or more than 45 years old.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of pain. Timepoint: 5 min, 15 min, 30 min 1 hour, 2 hour and 4 hour aftercaesarean section. Method of measurement: Verbal Numerical Rating Scale.