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A study to compare artificial initiation of the labour process with a rubber catheter on an out-patient basis with the standard process of initiation of labour with vaginal tablets after admission in the hospital

Phase 3
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2019/09/021132
Lead Sponsor
FLUID GRANT INSTITUTIONA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Low risk primi and multigravidas being induced for past dates

Exclusion Criteria

1.Previous LSCS

2.Hypertension, pre-eclampsia

3.IUGR, oligohydraminos

4.Diabetes

5.Low lying placenta

6.Chorioamnionitis or rupture of membranes

7.Bishop score more than 7

8.Primary or secondary infertility

9.Non- reactive NST

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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