Comparison of Cord Blood Lipid Profile among Hypertensive and Normotensive Mothers
Not Applicable
- Conditions
- Health Condition 1: O141- Severe pre-eclampsia
- Registration Number
- CTRI/2024/05/067148
- Lead Sponsor
- Divya Sinha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Singleton term pregnancy
2. Group A- women with gestational hypertension, chronic hypertension with superimposed pre-eclampsia, pre-eclampsia, eclampsia
3. Group B- normotensive women
Exclusion Criteria
1. Mothers with pre-existing medical conditions such as cardiovascular disorders, diabetes mellitus, collagen vascular diseases, HIV positive on HAART, known familial dyslipidemia, known case of pre-pregnancy hypertension
2. Non-vigorous baby at birth
3. Still Birth
4. Intra-Uterine Demise
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective- To estimate the cord blood lipid profiles in hypertensive and normotensive mothersTimepoint: 37 weeks to 42 weeks
- Secondary Outcome Measures
Name Time Method Secondary objective- To assess cord blood lipid profiles in relation to immediate materno-fetal outcomesTimepoint: 37 weeks to 42 weeks