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WINROP Algorithm Validation for Retinopathy Screening in a Cohort of Premature Infants — WINROP  

Retinopathy of Prematurity Clinical Trial

Official title:
WINROP Algorithm Validation for Retinopathy Screening in Premature Infants: a Retrospective Cohort Analysis Over 4 Years

Clinical Trial Summary

When a child was born too early, it is more likely to develop an alteration of its visual function than in the case of term birth. Significant visual disturbances are found in 3% of children born prematurely, but visual impairment can be very severe, up to the loss of vision in case of retinopathy of prematurity (ROP) in the most immature infants. The introduction of screening surveillance systems, such as WINROP software, might reduce the need for stressful eye examination in low risk neonates. This retrospective study aimed at validating the WINROP algorithm in a cohort of premature infants, born below 32 weeks of gestation, who had systematic eye examination for ROP screening over 4 year period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03347799
Study type Observational
Source Central Hospital, Nancy, France
Contact
Status Completed
Phase
Start date July 1, 2012
Completion date September 1, 2017
View Details
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