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effect of intra dermal and sub dermal injection of sterile water on active labor pai

Phase 3
Conditions
labor pain.
047.1
Registration Number
IRCT20170924036365N2
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

first pregnancy(nulliparyte)
dilatation of cervix 4cm or more
cephalic baby
gestational age 37w or more and planned for vaginal delivery

Exclusion Criteria

No inform consent
Multi parity
History of low back pain or abdominal pain unrelated to delivery
fetal demise
Skin lesion or infection on injection site
coagulation disorders of mother

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of pain. Timepoint: before intervention and 10,30,60,90, and 120 minute after intervention. Method of measurement: visual analogue scale.
Secondary Outcome Measures
NameTimeMethod
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