A study to observe the Effects of anti--Hypertensive drugs In pregnant wome
Not Applicable
- Conditions
- Health Condition 1: null- Pregnancy with hypertension
- Registration Number
- CTRI/2018/04/012950
- Lead Sponsor
- B J Medical College and Civil Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pregnant women with BP >= 140/90 mmHg.
Patient willing to give written informed consent
Exclusion Criteria
Pregnant women with BP < 140/90 mmHg
Patient not willing to give written informed consent
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method percentage of reduction of BPTimepoint: 4 months
- Secondary Outcome Measures
Name Time Method percentage of Adverse drug reactionsTimepoint: 4 months;percentage of IUGR and fetal distressTimepoint: 4 months;percentage of low birth weight babiesTimepoint: 4 months;percentage of maternal deathsTimepoint: 4 months;percentage of patients developing eclampsiaTimepoint: 4 months;percentage of perinatal deathsTimepoint: 4 months;percentage of preterm labourTimepoint: 4 months