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COMPLETED NA

Soy Formula Feedings in Healthy, Term Infants

NCT02456831 · View on ClinicalTrials.gov ↗

Study Summary

This study evaluates the GI tolerance and acceptability of soy formulas fed to healthy term infants with reported intolerance to a milk-based formula.

Conditions Studied

Interventions

  • OTHER Experimental Infant Formula 1
  • OTHER Experimental Infant Formula 2
  • OTHER Experimental Infant Formula 3
  • OTHER Active Comparator: Control Infant Formula

Study Locations (7)

Arkansas

  • Arkansas Children's Hospital — Little Rock

Illinois

  • Dreyer Clinic — Aurora

Kentucky

  • T&W Research — Owensboro

Minnesota

  • Park Nicollet Medical Foundation — Minneapolis

Ohio

  • Clinical Studies, Inc — Canton

Tennessee

  • Research Memphis — Memphis

Texas

  • Child Care Associates — San Antonio

Trial Details

FieldValue
Enrollment Target 115 participants
Start Date 1992-12
Est. Completion 1994-06
Phase NA

Sponsor

Abbott Nutrition

15 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02456831

The ClinicalTrials.gov registry entry for NCT02456831 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 115 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Nutrition, which has 15 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Gastrointestinal Tolerance appearing as the primary indexed condition, and to 4 interventions — of which Experimental Infant Formula 1 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02456831 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Arkansas, Illinois, Kentucky. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02456831 about?

NCT02456831 is a clinical study titled "Soy Formula Feedings in Healthy, Term Infants". This study evaluates the GI tolerance and acceptability of soy formulas fed to healthy term infants with reported intolerance to a milk-based formula.

What is the current status of trial NCT02456831?

This trial is currently completed. It is a NA study. The enrollment target is 115 participants. The study started on 1992-12. Estimated completion is 1994-06.

What conditions does trial NCT02456831 study?

This clinical trial studies the following conditions: Gastrointestinal Tolerance. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02456831?

The interventions under investigation include: Experimental Infant Formula 1 (OTHER), Experimental Infant Formula 2 (OTHER), Experimental Infant Formula 3 (OTHER), Active Comparator: Control Infant Formula (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02456831?

This trial is sponsored by Abbott Nutrition, which has 15 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02456831 being conducted?

This trial has 7 study locations across Arkansas, Illinois, Kentucky, Minnesota, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial