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Assessment of markers of Preeclampsia after delivery and correlation with future risk factors of CVD in women

Assessment of markers of Preeclampsia after delivery and correlation with future risk factors of Cardio vascular disease in women - CVD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/077771
Enrollment
225
Registered
2024-12-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O908- Other complications of the puerperium, not elsewhere classified

Interventions

Intervention1: Nil: Nil Control Intervention1: This is observational trial: This is observational trial

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Women over 18 years of age. 2. Diagnosed with hypertension during pregnancy (preeclampsia and gestational hypertension).

Exclusion criteria

Exclusion criteria: 1. History of chronic kidney disease, heart disease, diabetes with renal involvement or vasculopathy. 2. Pregnancy with chronic hypertension, other pre-existing medical conditions or history of illicit drug use. 3. Intervention that could modify the outcome like aspirin use.

Design outcomes

Primary

MeasureTime frame
1. We expect from this study to see the trend of inflammatory and biochemical markers in post delivery HDP women and to early predict risk factor of CVD later in life. 2. We expect that in this study to find, there is any difference between normalization of raised inflammatory marker and difference in biochemical marker 3. We will also do non invasive test (ETCO levels) and see the correlation with biomarkers. We hope to use these markers as screening tool for triaging women. 4. Most of these markers are assessed during antenatal period and very few studies are done in postpartum period. Of these sFlt1 and hCRP are specifically and strongly associated with development of CVD later in life. 5. Women who had hypertensive disorder in pregnancy with altered inflammatory markers may differentiate women at risk of developing hypertension a precursor of CVD later in life Timepoint: 1. We expect from this study to see the trend of inflammatory and biochemical markers in post delivery HDP women and to early predict risk factor of CVD later in life. 2. We expect that in this study to find, there is any difference between normalization of raised inflammatory marker and difference in biochemical marker 3. We will also do non invasive test (ETCO levels) and see the correlation with biomarkers. We hope to use these markers as screening tool for triaging women. 4. Most of these markers are assessed during antenatal period and very few studies are done in postpartum period. Of these sFlt1 and hCRP are specifically and strongly associated with development of CVD later in life. 5. Women who had hypertensive disorder in pregnancy with altered inflammatory markers may differentiate women at risk of developing hypertension a precursor of CVD later in life

Secondary

MeasureTime frame
1. We expect from this study to see the trend of inflammatory and biochemical markers in post delivery HDP women and to early predict risk factor of CVD later in life. 2. We expect that in this study to find, there is any difference between normalization of raised inflammatory marker and difference in biochemical marker 3. We will also do non invasive test (ETCO levels) and see the correlation with biomarkers. We hope to use these markers as screening tool for triaging women. 4. Most of these markers are assessed during antenatal period and very few studies are done in postpartum period. Of these sFlt1 and hCRP are specifically and strongly associated with development of CVD later in life. 5. Women who had hypertensive disorder in pregnancy with altered inflammatory markers may differentiate women at risk of developing hypertension a precursor of CVD later in life Timepoint: 6 WEEK, 6 MONTHS AND 12 MONTHS

Countries

India

Contacts

Public ContactDr Garima Kachhawa

All India Institute of Medical Sciences, New Delhi

garimakachhawa2012@gmail.com09868246702

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026