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Completed Not applicable Interventional

Use of Formula Fortified With DHA in Infants With Cystic Fibrosis

ClinicalTrials.gov ID: NCT00530244

Public ClinicalTrials.gov record NCT00530244. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 3:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Effect of Formula Fortified With Docosahexaenoic Acid (DHA) on Infants With Cystic Fibrosis (CF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The hypothesis of this study is that feeding infants diagnosed with CF via newborn screening a formula enhanced with a specific fish-oil fatty acid known as DHA will improve growth and decrease pancreatic dysfunction (as measured by human fecal elastase-1 in stool) over the first year of life. Briefly, infants diagnosed with CF in the first month of life whose parents chose not to breast feed their babies will be invited to enroll in a study comparing a standard commercial infant formula (Enfamil) with a formula enriched with arachidonic acid (AA) and docosahexaenoic acid (DHA). The study formula has 3 times the amount of DHA available in commercially available formulas. Infants will have monthly tests of stool elastase and blood work at entry, 3, 6, 9 and 12 months of age.

Study identification

NCT ID
NCT00530244
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
76 participants

Conditions and interventions

Interventions

Dietary Supplement

Eligibility (public fields only)

Age range
Up to 56 Days
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2003
Primary completion
Sep 30, 2011
Completion
Sep 30, 2011
Last update posted
Mar 6, 2018

2003 – 2011

United States locations

U.S. sites
24
U.S. states
12
U.S. cities
22
Facility City State ZIP Site status
UAB/CHS Cystic Fibrosis Center Birmingham Alabama 35233
Emory Cystic Fibrosis Center Atlanta Georgia 30322
Blank Children's Hospital Des Moines Iowa 50309
Cystic Fibrosis Care & Teaching Center Wichita Kansas 67218
Kosair Charities Louisville Kentucky 40202
Massachusetts General Hospital Boston Massachusetts 02114
Children's Hospital Boston Massachusetts 02115
Baystate Medical Center Springfield Massachusetts 01199
UMass Memorial Healthcare Worcester Massachusetts 01655
Children's Mercy Hospital Kansas City Missouri 64108
Monmouth Medical Center Long Branch New Jersey 07740
The Respiratory Center for Children Morristown New Jersey 07962-1956
Albany Medical Center Albany New York 12208
Children's Hospital Buffalo New York 14222
Schneider Children's Hospital New Hyde Park New York 11040
Strong Memorial Hospital Rochester New York 14642
Univesity Medical Center Stony Brook New York 11794
SUNY Upstate Medical Center Syracuse New York 13210
Children's Hospital at Westchester Medical Center Valhalla New York 10595
Lewis H Walker CF Pulmonary Center Akron Ohio 44308
Lewis H Walker Cystic Fibrosis Center Division of Pulmonary Akron Ohio 44308
St. Christopher's Hospital for Children Philadelphia Pennsylvania 19134
Children's Hospital of Pittsburgh Pittsburgh Pennsylvania 15231
Mountain State University Morgantown West Virginia 26506

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00530244, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 6, 2018 · Synced Sep 2, 2026

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The complete protocol, eligibility criteria, and contact information for NCT00530244 live on ClinicalTrials.gov.

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