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NCT01766011 · ClinicalTrials.gov registry record · Phase 2

Evaluation of a Standard Preterm Infant Formula Fed to Preterm Infants in the Hospital

A Phase 2 study, sponsored by Abbott Nutrition.

Completed
Registry status
Phase 2
Development phase
28
Enrollment target

NCT01766011: Completed Phase 2 study, sponsored by Abbott Nutrition.

NCT01766011 is a Phase 2 study that has completed, run by Abbott Nutrition. The registered enrollment target is 28 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01766011, a Phase 2 study, has completed, sponsored by Abbott Nutrition.

COMPLETED
Registry status
Phase 2
Development phase
28 participants
Enrollment target

Study Summary

The purpose of this study is to assess overall growth of preterm infants fed a reformulated preterm infant formula during hospitalization. All study products meet levels of nutrients for the infant population as specified in the Infant Formula Act and all subsequent amendments.

Primary Outcome

weight gain per day (g/kg/d)

Interventions

  • OTHER study pre-term formula

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2012-11
Est. Completion 2013-10
Phase Phase 2
Abbott Nutrition

89 total trials

What the finished NCT01766011 record still lists

NCT01766011 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower).

The record links to 0 conditions, and to 1 intervention - of which study pre-term formula is the first listed.

NCT01766011 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01766011 about?

NCT01766011 is a clinical study titled "Evaluation of a Standard Preterm Infant Formula Fed to Preterm Infants in the Hospital". The purpose of this study is to assess overall growth of preterm infants fed a reformulated preterm infant formula during hospitalization. All study products meet levels of nutrients for the infant population as specified in the Infant Formula Act and all subsequent amendments.

What is the current status of trial NCT01766011?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 28 participants. The study started on 2012-11. Estimated completion is 2013-10.

What interventions are being tested in trial NCT01766011?

The interventions under investigation include: study pre-term formula (OTHER).

Who is sponsoring clinical trial NCT01766011?

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

How this trial's enrollment target compares

Where NCT01766011's enrollment target sits among peer trials

28 1677th of 2000 higher than 304 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01766011, the US trial registry maintained by the National Library of Medicine. NCT01766011 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.