In pregnancies complicated with pre eclampsia there are various haemostatic parameters that are altered as compared to those patients whose bloodpressure readings are normal, so those parameters can be identified and pregnancies complicated with pre eclampsia can be managed before hand.
Not Applicable
- Conditions
- Health Condition 1: O149- Unspecified pre-eclampsia
- Registration Number
- CTRI/2021/03/032267
- Lead Sponsor
- DrArchana Suneja
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Gestational age 24 weeks to 40 weeks
pregnancy with singleton live foetus
No previous history of hypertension or pre eclampsia or eclampsia
Exclusion Criteria
Those women with
1.Hydatidiform Mole
2.Multifoetal Pregnancy
3.Intrauterine Foetal Demise
4.Diabetes Mellitus(Gestational or Overt)
Other Medical Conditions:
1.Essential Hypertension/Chronic
2.hypertension
3.Chronic Kidney Disease,
4.Cardiac Disorders
5.Connective Tissue Disease,
6.Autoimmune Disorders
7.Tuberculosis
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess if there are alterations in the various parameters of haemostatic assay in pre-eclamptic women as compared to normotensive pregnancies and to determine if these parameters are useful in the prediction of the severity of pre-eclampsia.Timepoint: 24 to 40 weeks
- Secondary Outcome Measures
Name Time Method 1.To evaluate the development of pre eclampsia in previously normotensive pregnant women. <br/ ><br>2.To assess the progression of mild pre eclamptic patients to severe pre eclampsia. <br/ ><br>3.To evaluate if there are significant alterations in parameters of haemostatic assay in mild as compared to severe pre eclampsia <br/ ><br>Timepoint: 24 to 40 weeks