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Trials / Completed

CompletedNCT02683317

Enteral Administration of Docosahexaenoic Acid to Prevent Retinopathy of Prematurity

Effect of Enteral Administration of Docosahexaenoic Acid on Development of the Retinopathy of Prematurity

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Coordinación de Investigación en Salud, Mexico · Other Government
Sex
All
Age
60 Minutes – 2 Weeks
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate whether docosahexaenoic acid given by enteral feeding prevent retinopathy of prematurity and/or diminish its severity in preterm infants.

Detailed description

Preterm neonates who start receiving enteral feeding will receive the intervention with docosahexaenoic acid (DHA) since the first day and throughout 14 days, one dose per day. The opthalmic evaluation will be done after 4-5 weeks after birth and followed until 42-45 corrected gestational age.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTdocosahexaenoic acidDocosahexaenoic acid is a dietary supplement derived from algae.
DIETARY_SUPPLEMENTsunflower oilSunflower similar to the excipient used in experimental group

Timeline

Start date
2016-02-22
Primary completion
2017-10-31
Completion
2017-10-31
First posted
2016-02-17
Last updated
2020-07-17

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT02683317. Inclusion in this directory is not an endorsement.

Enteral Administration of Docosahexaenoic Acid to Prevent Retinopathy of Prematurity (NCT02683317) · Clinical Trials Directory