the effect of hydralazine and nifedipine on hypertensio
Not Applicable
Recruiting
- Conditions
- preeclampsia.o14
- Registration Number
- IRCT20090701002114N6
- Lead Sponsor
- Khoram-Abad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.