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Role of serum biomarkers predicting neurological outcome in Birth asphyxia

Not Applicable
Conditions
Health Condition 1: null- Collecting venous blood sample and assessing serum biomarkers assay for correlating with neurological outcome and multiorgan dysfunction.
Registration Number
CTRI/2017/01/007739
Lead Sponsor
Institute of Child Health and Hospital for Children
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Neonates born at >=36 weeks of gestation and > 1800 gm birth weight with perinatal asphyxia are eligible. Perinatal asphyxia in patients born at the study

hospital or any other health facility was defined as the need for resuscitation at birth, along with the presence of one or more of the following.

1.Apgar score of <6 at 5 min after

birth,

2.Continued need for resuscitation, for > 5 mins

3.umbilical cord pH or any arterial pH of <7.00 within

60 min of birth and base deficit of >16 mmol/L within

60 min of birth

Exclusion Criteria

1.Babies with Major congenital anomalies

2.Babies arriving after 24 hours of age completed

3. Babies enrolled in Therapeutic Cooling Study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study correlation between s protein 100B,CARDIAC TROPONIN,CYSTATIN C,LDH with neurological outcome at 14 days and 90 days of ageTimepoint: 0,1,3,14,90 days
Secondary Outcome Measures
NameTimeMethod
To compare serum biomarkers against NICHD score in predicting neurological outcome. <br/ ><br> <br/ ><br>6. Study of correlation between MODS and neurological outcome at 14 days/later and 3months of age <br/ ><br> <br/ ><br>7. Neurological outcome at discharge by Hammersmith examination <br/ ><br> <br/ ><br>8. To compare above serum biomarkers against Mortality rate <br/ ><br>Timepoint: 0,1,3,14,90 days
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