Association of lateral location of placenta with development of high blood pressure in pregnancy
Not Applicable
- Conditions
- Health Condition 1: O149- Unspecified pre-eclampsia
- Registration Number
- CTRI/2024/01/062111
- Lead Sponsor
- self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Antenatal women belonging to 18-24 weeks of gestation with singleton pregnancy will be included in the study
Exclusion Criteria
Exclusion criteria
Women with chronic hypertension,
k/c/oDiabetes mellitus,
k/c/o Renal disease,
Severe anaemia,
k/c/oThyrotoxicosis,Gestational diabetes mellitus
Rh negative pregnancy
k/c/oImmunoinflammatory disease
k/c/o vascular disease
Patients with hemorrhagic disorders
k/c/o TORCH infections
Low-lying placenta
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess association of lateral location of placenta with development of pre-eclampsiaTimepoint: At the end of 18 months
- Secondary Outcome Measures
Name Time Method TO ASSESS ANY OBSTETRICS COMPLICATION ASSOCIATED WITH DEVELOPMENT OF PRE-ECLAMPSIATimepoint: AT END OF 18 MONTHS