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To measure biological markers in blood and urine sample of preterm babies

Not Applicable
Completed
Conditions
Health Condition 1: H351- Retinopathy of prematurity
Registration Number
CTRI/2019/10/021769
Lead Sponsor
Government medical college and hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
71
Inclusion Criteria

Group A include Neonates with Type 1 ROP

Group B include Neonates without any ROP matched by gestation within 1 week for neonates enrolled in group A

Exclusion Criteria

Infants with Congenital abnormalities

Infants born to mother with gestational metabolic diseases

TORCH infections suspicion on eye examination

Hydrocephalus

Necrotising enterocolitis

Periventricular leukomalacia

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare inflammatory (Interleukin-6 and Interleukin-8) and angiogenic (Vascular endothelial growth factor) biomarkers in preterm babies with or without Type 1 Retinopathy of prematurity <br/ ><br>To study the association of systemic biomarkers with the stage and zone of Retinopathy <br/ ><br>of prematurity <br/ ><br> <br/ ><br>Timepoint: AT 18 months
Secondary Outcome Measures
NameTimeMethod
ILTimepoint: NI
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