Pregnancy outcomes with chronic hypertetion on different antihypertensive therapy
Phase 1
Completed
- Conditions
- Preeclampsia.Gestational [pregnancy-induced] hypertension
- Registration Number
- IRCT201602067676N5
- Lead Sponsor
- Vice Chancellor for Research and Technology University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Inclusion criterion: pregnant women with chronic hypertension.
Exclusion criteria: absence of consent to participate.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Added preeclampsia. Timepoint: During prenatal visits. Method of measurement: Manometer.
- Secondary Outcome Measures
Name Time Method Placental abruption. Timepoint: During pregnancy. Method of measurement: Physical examination.;Fetal death. Timepoint: During pregnancy. Method of measurement: Ultrasound.;Acute kidney injury. Timepoint: During pregnancy. Method of measurement: Physical examination.;Cerebral hemorrhage. Timepoint: During pregnancy. Method of measurement: Physical examination.