Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Nutritional Study in Preterm Infants
NCT00707837 · View on ClinicalTrials.gov ↗
Study Summary
An evaluation of a preterm infant formula containing ingredients similar to those found in breastmilk
Conditions Studied
Interventions
- OTHER Preterm infant formulas and discharge formulas
- OTHER Preterm infant formula with added soluble lipids
Study Locations (8)
Florida
- West Coast Neonatalogy, All Children's Hospital — St. Petersburg
- University of South Florida — Tampa
Alabama
- University of Alabama — Birmingham
Kentucky
- University of Louisville — Louisville
New York
- Maria Fareri Children's Hospital at Winchester Medical Center — Vahalla
Ohio
- MetroHealth Medical Center — Cleveland
Rhode Island
- Women & Infants Hospital of Rhode Island — Providence
Utah
- University of Utah — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 206 participants |
| Start Date | 2005-05 |
| Est. Completion | 2008-08 |
| Phase | Phase 3 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00707837
The ClinicalTrials.gov registry entry for NCT00707837 describes a study currently listed as completed. It is categorized as Phase 3, 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 206 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 Preterm Infants appearing as the primary indexed condition, and to 2 interventions — of which Preterm infant formulas and discharge formulas 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: NCT00707837 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Florida, Alabama, 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 NCT00707837 about?
NCT00707837 is a clinical study titled "Nutritional Study in Preterm Infants". An evaluation of a preterm infant formula containing ingredients similar to those found in breastmilk
What is the current status of trial NCT00707837?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 206 participants. The study started on 2005-05. Estimated completion is 2008-08.
What conditions does trial NCT00707837 study?
This clinical trial studies the following conditions: Preterm Infants. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00707837?
The interventions under investigation include: Preterm infant formulas and discharge formulas (OTHER), Preterm infant formula with added soluble lipids (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00707837?
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 NCT00707837 being conducted?
This trial has 8 study locations across Alabama, Florida, Kentucky, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.