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An observational study of coagulation profile in severe pre eclampsia and eclampsia patients

An observational study of coagulation profile in severe pre-ecampsia and eclampsia patients. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/07/069840
Enrollment
74
Registered
2024-07-03
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: O141- Severe pre-eclampsia

Interventions

Intervention1: NIL: NIL

Sponsors

Spurthi Prabhakar self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: hypertensive females

Exclusion criteria

Exclusion criteria: pregnant female with known history of pre hypertensive disorder on anticoagulant therapy established DIC intrauterine fetal demise. history of bleeding disorder abruptio placentae

Design outcomes

Primary

MeasureTime frame
platelet count decreases PT and APTT is prolongedTimepoint: The values will be observed in period of gestation between 20 weeks to 40 weeks , in the above gestational period whenever patients arrives with symptoms of severe pre eclampsia and eclampsia—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactSpurthi Prabhakar

Jawaharlal Nehru medical college , Belgavi

anitamgan@gmail.com9440969906

Outcome results

None listed

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