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Study of correlation of ductus venous doppler changes and fetal outcome in pregnant women with pre-ecclampsia

A prospective observational study of correlation of ductus venous doppler and fetal outcome in Pre-ecclampsia - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/093117
Enrollment
78
Registered
2025-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: O140- Mild to moderate pre-eclampsia

Interventions

Control Intervention1: NIL: NIL

Sponsors

Shri B M Patil medical college hospital and research centre Vijayapura
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: pregnant women with preeclampsia between 34-40 weeks period of gestation, singleton pregnancy, no underlying medical conditions

Exclusion criteria

Exclusion criteria: patients with fetal anomalies, patients with other medical conditions (dm, htn, respiratory, cardiac, renal, liver diseases), patients with chronic hypertension, gestational hypertension, multifetal pregnancy, uncertain gestational age, patients with preeclampsia who are prescribed low molecular weight heparin or aspirin

Design outcomes

Primary

MeasureTime frame
to assess the association between ductus venous doppler changes and perinatal outcomeTimepoint: on the day 1 of fetal life—

Secondary

MeasureTime frame
to assess the association between ductus venous doppler & maternal obstetric outcomeTimepoint: on post operative day immediate—

Countries

India

Contacts

Public ContactDr Vinaya Patil

Shri B. M. Patil medical college hospital and research centre

drsrbidri1@gmail.com9880162550

Outcome results

None listed

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