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NCT00707837 · ClinicalTrials.gov registry record · Phase 3

Nutritional Study in Preterm Infants

A Phase 3 study of Preterm Infants, sponsored by Abbott Nutrition.

Completed
Registry status
Phase 3
Development phase
206
Enrollment target
8
Study locations

NCT00707837 is a Phase 3 study of Preterm Infants that has completed, run by Abbott Nutrition. The registered enrollment target is 206 participants. The trial reports 8 study locations across 7 states.

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The verdict

NCT00707837, a Phase 3 study of Preterm Infants, has completed, sponsored by Abbott Nutrition.

COMPLETED
Registry status
Phase 3
Development phase
206 participants
Enrollment target
8
Study locations

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

FieldValue
Enrollment Target 206 participants
Start Date 2005-05
Est. Completion 2008-08
Phase Phase 3

Sponsor

Abbott Nutrition

89 total trials

What the Registry Record Tells You About NCT00707837

The ClinicalTrials.gov registry entry for NCT00707837 describes a study currently listed as completed, categorized as Phase 3. 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 89 total studies on file at ClinicalTrials.gov.

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.

NCT00707837 reports 8 study locations spanning 7 distinct geographic areas - top geographies include Florida, Alabama, Kentucky.

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.

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).

Who is sponsoring clinical trial NCT00707837?

This trial is sponsored by Abbott Nutrition, which has 89 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Preterm Infants

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.