Skip to content

IV Labetalol Vs Oral Nifedipine in control of severe hypertension in pregnancy

IV Labetalol and Oral Nifedipine in acute control of severe hypertension in pregnancy- A comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/009977
Enrollment
120
Registered
2017-10-03
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: null- Pregnancy with PreEclampsia

Interventions

Intervention1: Intravenous Labetalol: Combined alpha plus beta blocker for severe hypertension in pregnancy. Patients randomized to intravenous labetalol received 20 mg initially followed by escalatin

Sponsors

Government Siddhartha Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All antenatal women of gestational age >28 weeks with severe hypertension with systolic blood pressure (BP) of 160 mm Hg or higher and/or diastolic BP of 110 mm Hg or higher on 2 separate occasions 30 minutes apart in lateral recumbent position

Exclusion criteria

Exclusion criteria: 1. Patients with history of cardiac disease 2. Patients with history of bronchial asthma 3. Patients with history of haematological disorder 4. Patients with history of allergy to labetalol or nifedipine 5. Patients with liver disorders 6. Maternal heart rate 120 bpm 7. Patients with history of exposure to any anti-hypertensive medications in the past 24 hours 8. Patients with chronic hypertension

Design outcomes

Primary

MeasureTime frame
The time taken in minutes,by either drug to achieve the target blood pressure of systolic BP 150mmHg and/or diastolic BP 110mmHg.Timepoint: Mean time taken to achieve target blood pressures in a set study population for a period of two years

Secondary

MeasureTime frame
The number of doses required Adverse effects Maternal and perinatal oucomeTimepoint: mean number of doses required, adverse effects and maternal and perinatal outcome in a set study population at the end of 2 years

Countries

India

Contacts

Public ContactMomina Zulfeen

Govt. Siddhartha Medical College

radhatatapudi@gmail.com9849666803

Outcome results

None listed

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