FindTrial
Sign In

Outcomes of induction of labour in pregnancy

Association of plasma leptin levels with outcome of induction of labour in pregnant women - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/12/060836
Enrollment
180
Registered
2023-12-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O619- Failed induction of labor, unspecified

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Dr Priya Lal
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: Multiple gestation Fetal anomalies Augmentation of labour rather than induction of labour Intrauterine fetal death

Design outcomes

Primary

MeasureTime frame
1. Maternal plasma Leptin levels 2.Success or failure of Induction of labour 3.Mode of delivery 4.Fetal birth weight 5.Fetal APGAR 6.Admission to NICU 7.Administration of neonatal antibiotics Timepoint: From 37 weeks POG till 2 weeks postnatally—

Secondary

MeasureTime frame
1. Fetal birth weight 2.Fetal APGAR 3.Admission to NICU 4.Administration of neonatal antibiotics Timepoint: From 37 weeks POG till 2 weeks postnatally—

Countries

India

Contacts

Public ContactDr Monika Gupta

VARDHMAN MAHAVIR MEDICAL COLLEGE AND SAFDARJUNG HOSPITAL

priyalal.8@gmail.com09971855774

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026