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A study to associate the iron profile values estimated during early pregnancy with the onset of hypertensive disorders of pregnancy

A Prospective cohort study of Iron profile values estimated during early pregnancy and their correlation with the onset of hypertensive disorders of pregnancy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/083851
Enrollment
100
Registered
2025-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: O10-O16- Edema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium

Interventions

Control Intervention1: NIL: NIL

Sponsors

Shri B M Patil Medical College Hospital and Research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All singleton pregnant women within 18-30 age group with periods of gestation equal to or more than 12 weeks and less than or equal to 19 weeks and six days.

Exclusion criteria

Exclusion criteria: 1.Chronic hypertensive patients 2.Known case of chronic infections. 3.Known case of malignancies. 4.Known case of Liver, Renal or cardiac disease. 5.Known case of hemochromatosis. 6.H/O past blood transfusions or parenteral iron infusions in the last 3 months. 7.Known case of hemoglobinopathies. Pregnancy with anomalous babies. 8.H/O anemia with Hb less than 11g/dl

Design outcomes

Primary

MeasureTime frame
1.To associate iron profile levels estimated during early pregnancy with the onset of hypertensive disorders of pregnancy. 2.Gestational age at the time of development of hypertensive disorders of pregnancy. pregnancyTimepoint: 1.The women taken into the study are followed from 12 weeks to the time of delivery to look for any hypertensive disorders of pregnancy

Secondary

MeasureTime frame
Maternal outcome: a] Gestational age at delivery b] Mode of delivery c] Any other outcomes The neonatal outcome: d] Weight e] NICU admission f] Neonatal death Timepoint: The women taken into the study are followed from 12 weeks to the time of delivery to look for any hypertensive disorders of pregnancy and the neonatal outcomes are recorded

Countries

India

Contacts

Public ContactSREE KAVYA MEDA

SHRI B M PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTRE

neelamma.patil@bldedu.ac.in9845068074

Outcome results

None listed

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