Hs CRP level in pre eclampsia
Not Applicable
- Conditions
- Health Condition 1: O140- Mild to moderate pre-eclampsia
- Registration Number
- CTRI/2024/04/065086
- Lead Sponsor
- Chintakindi Preethi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. All preeclamptic pregnant women who are admitted in antenatal ward or labour room
2. Singleton pregnancy
3. Pre eclamptic women willing to participate in the study
Exclusion Criteria
1. Preeclamptic women with history of fever or recent infections or who are receiving antibiotic treatment or steroids.
2. Preeclamptic women in labour or presenting with PROM or clinical chorioamnionitis.
3. Preeclamptic women with chronic inflammatory disorders like arthritis, inflammatory bowel disorders, SLE etc.
4. Preeclamptic women with medical disorders (Diabetes mellitus, hepatic disorders, renal disorders)
5. Pregnant women whose BMI > 25kg/m2
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study high sensitive c reactive protein levels in early onset pre ecclampsia and late onset pre ecclampsia in pregnancyTimepoint: 20 weeks - 40 weeks
- Secondary Outcome Measures
Name Time Method Fetomaternal outcome in raised hsCRP LevelsTimepoint: 1 month