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A comparative study of effects of Entonox versus Epidural Analgesia on stages of labor, maternal & fetal outcome and pain relief when used as labor analgesia in singleton pregnancy

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: 1- Obstetrics
Registration Number
CTRI/2023/04/051802
Lead Sponsor
Command Hospital Air Force Bangalore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Pregnant women aged between 18 years and 35 years with singleton cephalic pregnancy at gestational age between 37 to 42 weeks, brought in labour at cervical dilatation of 4 cm

Exclusion Criteria

•Any case for which normal vaginal delivery is contraindicated.

•Patients with Pre-Eclampsia, Heart diseases, Abnormal Placentation, FGR, Post LSCS Pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
(a)To compare the duration of 1st, 2nd and 3rd stage of labor <br/ ><br> <br/ ><br>(b)To compare the pain relief between Nitrous Oxide and Epidural Analgesia using pain scale from 0-10 <br/ ><br>Timepoint: Intra partum
Secondary Outcome Measures
NameTimeMethod
(a)The mode of the delivery between nitrous oxide and epidural analgesia - Normal Vaginal/Assisted/ cesarean <br/ ><br> <br/ ><br>(b)Adverse maternal outcome between nitrous oxide and epidural analgesia <br/ ><br> <br/ ><br>(c)Fetal outcomes in terms of APGAR score of newborns, need for resuscitation and NICU admissionTimepoint: Intra Partum and Post Partum
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