A one year study to determine the maternal and fetal outcomes in pregnant women with heart disease
Not Applicable
- Conditions
- Health Condition 1: O098- Supervision of other high risk pregnancies
- Registration Number
- CTRI/2019/03/018083
- Lead Sponsor
- Dr Lameez Khan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All pregnant women more than 20 weeks period of gestation admitted with known or newly diagnosed cardiac disease (congenital or acquired) whether symptomatic or asymptomatic
Exclusion Criteria
- all pregnant women with cardiac disease admitted for termination of pregnancy
- cardiac disease in which pregnancy is contraindicated like Eisenmengers syndrome
incomplete records of the patient
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the feto-maternal outcomes in all pregnant women with heart diseaseTimepoint: Mode of delivery <br/ ><br>Maternal outcome and complications - CHF,AF,IE, Cardiac complications <br/ ><br>Fetal outcomes- NICU admission , SGA, IUGR, Prematurity, birth asphyxia, birth weight, IUFD
- Secondary Outcome Measures
Name Time Method To determine the feto-maternal outcomes in all pregnant women with heart diseaseTimepoint: Mode of delivery <br/ ><br>Maternal outcome and complications - CHF,AF,IE, Cardiac complications <br/ ><br>Fetal outcomes- NICU admission , SGA, IUGR, Prematurity, birth asphyxia, birth weight, IUFD