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the effect of hydralazine and nifedipine on hypertension

Comparative study of the effect of hydralazine and nifedipine on acute hypertension in women with preeclampsia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090701002114N6
Enrollment
60
Registered
2020-09-21
Start date
2020-09-12
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

preeclampsia. o14

Interventions

Intervention 1: Intervention group: In intervention group number one, which includes receiving hydralazine. 5 mg of this drug will be slowly injected intravenously and to blind the samples in this gro

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women 18 to 45 years old Gestational age greater than or equal to 20 weeks Blood pressure greater than or equal to 160 over 110

Exclusion criteria

Exclusion criteria: Maternal disease of any kind, including heart (heart arrhythmia - heart failure - chest pain, etc.), kidney, liver Fetal disorders including intrauterine growth restriction (IUGR) and Oligohydramnios Uncertain patterns of fetal heart rate

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure. Timepoint: At the beginning of the study, then every twenty minutes until the blood pressure drops. Method of measurement: Using electronic blood pressure monitoring device.;Diastolic blood pressure. Timepoint: At the beginning of the study, then every twenty minutes until the blood pressure drops. Method of measurement: Using electronic blood pressure monitoring device.

Secondary

MeasureTime frame
Average blood pressure. Timepoint: At the beginning of the study, then every twenty minutes until the blood pressure drops. Method of measurement: Using electronic blood pressure monitoring device.;Time to achieve controlled blood pressure. Timepoint: At the beginning of the study, then every twenty minutes. Method of measurement: Used in hours and in minutes.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Yari

Khoram-Abad University of Medical Sciences

yari.f@lums.ac.ir+98 66 3312 0133

Outcome results

None listed

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