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To study the effect of anaesthesia given during cesarean section in patients having high blood pressure during pregnancy on the blood supply to the fetus.

Phase 3
Conditions
Health Condition 1: null- preeclamptic femaes undergoing cesarean section
Registration Number
CTRI/2018/02/012096
Lead Sponsor
PGIMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

25 normal and 25 severely preeclamptic pregnant women with singleton gestation scheduled for elective CD under SA

Exclusion Criteria

chronic hypertension, coagulopathy, multiple gestation, in labor or fetal distress, will be excluded from the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
doppler indices values-PI,RI and SD ratiTimepoint: doppler indices values-10 minutes before and 10 minutes after spinal anaesthesia
Secondary Outcome Measures
NameTimeMethod
neonatal arterial and venous blood gases,apgar scoreTimepoint: just after birth
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