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Sublingual misoprostol vs intracervical foleys catheter f/b misoprostol forinduction of labor in primigravida

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2023/04/051747
Lead Sponsor
Poojan Dogra
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

All primigravida women reporting to delivery area requiring induction of labour at term.

Exclusion Criteria

1)Breech presentation/ Transverse lie/ Twin pregnancy/ Placenta praevia/ Any other

contraindication for vaginal delivery.

2)Multipara

3)Any evidence of active labour or intrauterine infection, uterine scarring, hypersensitivity to

misoprostol

4)Any systemic comorbidity (cardiovascular disease, kidney disease, asthma, etc.), fetal

macrosomia, non-reassuring fetal heart rate in nonstress test (NST)

5)Known allergic to latex

6)Not willing to participate in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare vaginal delivery rate in both groupsTimepoint: Baseline then every four hourly.
Secondary Outcome Measures
NameTimeMethod
See outcome in terms of adverse effect to mother/baby.Timepoint: During labor process and after delivery.
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