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Relation between uric acid in blood and in saliva of patients with high BP recordings in pregnancy and in normal pregnancy.

Phase 2
Conditions
Health Condition 1: O140- Mild to moderate pre-eclampsia
Registration Number
CTRI/2020/12/029693
Lead Sponsor
Kasturba Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

pregnant women with or without pre-eclampsia at the gestation of 20 weeks and above

Exclusion Criteria

multiple pregnancy, diabetes mellitus, chronic

hypertension, any other cardiovascular disease, gout, connective tissue

disorder, renal or liver disease, history of thromboembolism, history of any

chronic illness, neural tube defect and other congenital malformation, patients

with oral infection, poor oral hygiene and recent oral injuries, Maternal or fetal

indication for iatrogenic preterm delivery

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess if there is correlation between serum and salivary uric acid with each other and with pre-eclampsia and to assess their relation with neonatal outcome.Timepoint: Salivary uric acid and serum uric acid once at the time of diagnosis of pre-eclampsia ( 20weeks gestation or above) <br/ ><br> <br/ ><br>Neonatal outcome at delivery
Secondary Outcome Measures
NameTimeMethod
If salivary uric acid can be used as a non invasive spot test for predicting pre-eclampsia in pregnant women.Timepoint: Salivary and serum uric acid at the time of diagnosis of pre-eclampsia (20 weeks of gestation or more) <br/ ><br> <br/ ><br>Neonatal outcome at time of delivery
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