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A study of outcomes of artificially starting the process of labour in mothers with too little fluid (amniotic fluid) surrounding the baby in the uterus.

Not Applicable
Conditions
Health Condition 1: O410- Oligohydramnios
Registration Number
CTRI/2021/04/032602
Lead Sponsor
G Aparna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients planned for induction of labour and satisfying the below criteria

1.Antenatal women between 18 and 35 years

2.Gestational age between 37 weeks and 42 weeks

3.AFI <=5

4.Singleton pregnancy with cephalic presentation

5.Bishopâ??s score <6

Exclusion Criteria

1.Women with pre labour rupture of membranes

2.Major congenital anomalies in fetus

3.Multifetal gestation

4.Abnormal lie and presentation

5.Maternal complications like cardiovascular disease and maternal pulmonary disorder

6.Conditions which preclude a vaginal delivery

7.Women planned for elective caesarean section.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mode of delivery <br/ ><br>Induction to delivery interval <br/ ><br>Apgar scoresTimepoint: In labour <br/ ><br>At delivery <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Meconium staining of amniotic fluid <br/ ><br>Low birth weight <br/ ><br>Neonatal intensive care unit (NICU) admission <br/ ><br>Length of NICU stayTimepoint: In labour <br/ ><br>At delivery <br/ ><br>Immediately after delivery <br/ ><br>Four days after delivery <br/ ><br>At discharge from hospital
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