Comparison of adding sufentanil and dexamethasone to ropivacaine 0.1% in painless labor

Phase 3

Recruiting

• Conditions: Painless labor.; Spontaneous vertex delivery; O80.0

• Registration Number: IRCT20220912055952N1
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 November 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 104

Inclusion Criteria

Term pregnancy
Singleton pregnancy

Exclusion Criteria

Allergy to any of the drugs used
The presence of spinal deformities
Presence of coagulopathy
History of heart/pulmonary/kidney/liver disease

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of pain relief. Timepoint: At 15, 30 and 60 minutes after epidural injection. Method of measurement: Visual Analogue Scale of pain.

Secondary Outcome Measures

Name	Time	Method
Headache. Timepoint: Up to 6 hours after delivery. Method of measurement: Clinical interview.;Nausea. Timepoint: Up to 6 hours after delivery. Method of measurement: Clinical interview.