FindTrial
Sign In

Neonatal Outcome In Meconium Stained Amniotic Fluid A Cross sectional Study

Perinatal Outcome In Meconium Stained Liquor A Cross Sectional Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/02/062746
Enrollment
155
Registered
2024-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O419- Disorder of amniotic fluid and membranes, unspecified Health Condition 2: O419- Disorder of amniotic fluid and membranes, unspecified

Interventions

Control Intervention1: NIL: NIL

Sponsors

ROHILKHAND MEDICAL COLLEGE HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All pregnant females with term pregnancies, cephalic presentation and singleton pregnancy

Exclusion criteria

Exclusion criteria: Congenital malformation Intrauterine fetal death Breech presentation Oligphydroamnios

Design outcomes

Primary

MeasureTime frame
To assess maternal and perinatal outcome in patients with meconium stained liquor during labourTimepoint: To assess maternal and perinatal outcome in patients with meconium stained liquor during labour—

Secondary

MeasureTime frame
To determine the association of meconium stained amniotic fluid with abnormal CTG during labourTimepoint: 37-42 weeks—

Countries

India

Contacts

Public ContactDr Tripti Gupta

Rohilkhand Medical College Hospital

dr.triptigupta@rediffmail.com8433288211

Outcome results

None listed

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