Completed

Phase 3
Age: 0 - 1Day
All Genders
ID00000156

The Effects of Light Reduction on Retinopathy of Prematurity (Light-ROP)

Led by National Eye Institute (NEI) · Updated on 2006-06-05

N/A

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

To evaluate the effect of ambient light reduction on the incidence of retinopathy of prematurity (ROP).

CONDITIONS

Brief Title

The Effects of Light Reduction on Retinopathy of Prematurity (Light-ROP)

Who Can Participate

Age: 0 - 1Day
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

Premature infants weighing less than 1,251 grams at birth and having a gestational age of less than 31 weeks were eligible for randomization. Consent must have been obtained within 24 hours of birth. Patients with major congenital anomalies are excluded.

Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Total: 3 locations

1

The Children's Hospital of Buffalo

Buffalo, New York, United States

Status Unknown

2

The University of Texas, Southwestern Medical Center at Dallas

Dallas, Texas, United States

Status Unknown

3

University of Texas, Health Science Center, San Antonio

San Antonio, Texas, United States

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

N/A

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial

Lack of efficacy of light reduction in preventing retinopathy of prematurity. Light Reduction in Retinopathy of Prematurity (LIGHT-ROP) Cooperative Group.

J D Reynolds, R J Hardy, K A Kennedy...

https://pubmed.ncbi.nlm.nih.gov/9603794