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To study how the severity of preeclampsia in pregnant females is associated with changes in blood parameters and biochemical parameters

A study on association of hematological and biochemical indices with disease severity in preeclampsia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/082530
Enrollment
280
Registered
2025-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: O149- Unspecified pre-eclampsia

Interventions

None listed

Sponsors

Priyanka Katiyar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Singleton pregnancy with diagnosed preeclampsia

Exclusion criteria

Exclusion criteria: Women with multiple gestation Women with diabetes mellitus Women with chronic hypertension Women with pre-existing renal disease, cardiovascular disease, liver disease, dyslipidemia,any thyroid disease Women with active labour, PROM, polyhydramnios, severe anemia, IUD Women with infectious diseases diagnosed during pregnancy Women having chronic inflammatory disease

Design outcomes

Primary

MeasureTime frame
It might be possible to predict the severity of preeclampsia by platelet indices, liver function test, renal function test and thyroid stimulating hormone.Timepoint: 1 year—

Secondary

MeasureTime frame
Preeclampsia whether severe or non severe might lead to preterm delivery & risk of preeclampsia in subsequent pregnanciesTimepoint: 1 year—

Countries

India

Contacts

Public ContactDr Dolly Rastogi

Gsvm medical College

drdollyrastogi@gmail.com8400331162

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026