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To study the fetomaternal outcome of decreased sodium level in the patients of one of the subtypes of hypertensive disorders in pregnancy and its association with the severity of the disorder

To study the correlation of hyponatremia with the fetomaternal outcome in patients of preeclampsia with severe features and to study its association as a marker of the severity of preeclampsia - HOPE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/07/034561
Enrollment
100
Registered
2021-07-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Pregnant women with the period of gestation between 20 to 40 weeks admitted in labour ward with blood pressure more than or equal to 140/90 mmHg measured on 2 occasions 4 hours apart consenting to be enrolled in study. 2)Age more than or equal to 18 years 3)All patients falling under the ACOG Criteria for severe Preeclampsia

Exclusion criteria

Exclusion criteria: 1)Pregnant women who do not consent for study 2)Women with chronic kidney disease, liver disease, cardiovascular disease, collagen vascular disease, chronic hypertension, diabetes, neoplasm, with major fetal anomaly, endocrine disorders causing electrolyte imbalance, CNS disorders, on steroids /diuretics

Design outcomes

Primary

MeasureTime frame
1) Fetomaternal outcome in preeclamptic patients with severe features presenting with hyponatremia 2) Association of hyponatremia with the severity of preeclampsiaTimepoint: 1 year

Secondary

MeasureTime frame
Proportion of hyponatremia in preeclamptic patients with severe featuresTimepoint: 1 YEAR

Countries

India

Contacts

Public ContactRamya Lasmi R

Postgraduate Institute of Medical Education and Research

drseemachopra@yahoo.com7087009351

Outcome results

None listed

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