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Completed Not applicable Interventional Accepts healthy volunteers

Growth of Infants Fed an Extensively Hydrolyzed Infant Formula

ClinicalTrials.gov ID: NCT01210391

Public ClinicalTrials.gov record NCT01210391. 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 Oct 28, 2026, 3:30 AM EDT

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

Official title

Assessment of Growth of Infants Fed a 100% Whey Extensively Hydrolyzed Formula.

Brief summary

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

The primary objective of the clinical trial is to compare growth in infants (expressed as weight gain in g/day) consuming a new extensively hydrolyzed formula (EHF) to infants consuming a commercially available EHF.

Study identification

NCT ID
NCT01210391
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
282 participants

Conditions and interventions

Eligibility (public fields only)

Age range
11 Days to 4 Months
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Nov 2010 (Type not available)
Primary completion
Jul 2013 (Actual)
Completion
Jul 2013 (Actual)
Last update posted
Jun 26, 2014

2010 – 2013

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Colorado Springs Health Partners Colorado Springs Colorado — —
Pedia Research Newburgh Indiana 42301 —
Pedia Research Owensboro Kentucky 42301 —
ARK-LA-Tex Pediatric Research Bossier City Louisiana — —
The Clinical Trials Center New Orleans Louisiana 70118 —
Clinical Research of Nevada Las Vegas Nevada — —
Institute of Clinical Research Mayfield Heights Ohio — —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Cyn3rgy Research Gresham Oregon — —
Square-1 Clinical Research Erie Pennsylvania — —
Alpha Clinical Research Clarksville Tennessee — —
Jackson Clinic Jackson Tennessee 38305 —
Scott & White Wells Branch Clinic Austin Texas 78728 —
Scott & White Killeen Clinic Killeen Texas 76543 —
DCOL Center for Research Longview Texas — —
Southwest Children's Research Associates San Antonio Texas 78229 —
Scott & White Temple Temple Texas 76508 —
Tanner Clinic Layton Utah — —
Clinical Research Partners Richmond Virginia — —
Wenatchee Valley Medical Center Wenatchee Washington — —

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 NCT01210391, 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 Jun 26, 2014 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01210391 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →