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Comparison effect of Entonox and Dexamethasone

Phase 3
Conditions
Painful delivery.
Registration Number
IRCT20190924044865N1
Lead Sponsor
Ardabil University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

First Pregnancy
Term pregnancy
Without illness

Exclusion Criteria

preterm laber
multipar

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score. Timepoint: 30, 60, 120, 180 minutes. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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