Outcomes of induction of labour in pregnancy
Not Applicable
- Conditions
- Health Condition 1: O619- Failed induction of labor, unspecified
- Registration Number
- CTRI/2023/12/060836
- Lead Sponsor
- Dr Priya Lal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All antenatal women at more than or equal to 37 weeks of gestation who have undergone induction of labour by any method (misoprostol, dinoprostone, PGE2 gel, oxytocin, artificial rupture of membranes, membrane stripping or Foley’s balloon placement)
Exclusion Criteria
Multiple gestation
Fetal anomalies
Augmentation of labour rather than induction of labour
Intrauterine fetal death
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Maternal plasma Leptin levels <br/ ><br>2.Success or failure of Induction of labour <br/ ><br>3.Mode of delivery <br/ ><br>4.Fetal birth weight <br/ ><br>5.Fetal APGAR <br/ ><br>6.Admission to NICU <br/ ><br>7.Administration of neonatal antibiotics <br/ ><br>Timepoint: From 37 weeks POG till 2 weeks postnatally <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. Fetal birth weight <br/ ><br>2.Fetal APGAR <br/ ><br>3.Admission to NICU <br/ ><br>4.Administration of neonatal antibiotics <br/ ><br>Timepoint: From 37 weeks POG till 2 weeks postnatally <br/ ><br>