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NCT00872664 · ClinicalTrials.gov registry record · NA
Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented With Carotenoids
A NA study of Retinopathy of Prematurity, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT00872664 is a NA study of Retinopathy of Prematurity that has completed, run by University of Utah. The registered enrollment target is 36 participants, below the 364-participant average among 7 other Retinopathy of Prematurity trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00872664, a NA study of Retinopathy of Prematurity, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objectives of this study are to compare the serum and skin concentrations of beta-carotene, lutein, and lycopene in preterm infants fed preterm formulas with mixed carotenoids to serum concentrations in preterm infants fed preterm formulas with no added carotenoids and to human milk fed infants. The secondary objective of this study is to evaluate the effects of dietary carotenoids on the developing eye. Stages and zones of retinopathy of prematurity (ROP), retinal function, and retinal characteristics will also be examined.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT carotenoids
Study Locations (1)
Utah
- University of Utah Health Sciences Center - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2009-09 |
| Est. Completion | 2013-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00872664
The ClinicalTrials.gov registry entry for NCT00872664 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 364-participant average among 7 other Retinopathy of Prematurity trials with a reported enrollment target (90% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Retinopathy of Prematurity appearing as the primary indexed condition, and to 1 intervention - of which carotenoids is the first listed.
NCT00872664 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.
Frequently Asked Questions
What is clinical trial NCT00872664 about?
NCT00872664 is a clinical study titled "Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented With Carotenoids". The primary objectives of this study are to compare the serum and skin concentrations of beta-carotene, lutein, and lycopene in preterm infants fed preterm formulas with mixed carotenoids to serum concentrations in preterm infants fed preterm formulas with no added carotenoids and to human milk fed ...
What is the current status of trial NCT00872664?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2009-09. Estimated completion is 2013-06.
What conditions does trial NCT00872664 study?
This clinical trial studies the following conditions: Retinopathy of Prematurity.
What interventions are being tested in trial NCT00872664?
The interventions under investigation include: carotenoids (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT00872664?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00872664 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
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