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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | docosahexaenoic acid | Docosahexaenoic acid is a dietary supplement derived from algae. |
| DIETARY_SUPPLEMENT | sunflower oil | Sunflower 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.