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NCT01155414 · ClinicalTrials.gov registry record · Phase 3
Tolerance of Healthy Term Infants Fed Infant Formulas #4
A Phase 3 study, sponsored by Abbott Nutrition.
- Completed
- Registry status
- Phase 3
- Development phase
- 168
- Enrollment target
NCT01155414: Completed Phase 3 study, sponsored by Abbott Nutrition.
NCT01155414 is a Phase 3 study that has completed, run by Abbott Nutrition. The registered enrollment target is 168 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01155414, a Phase 3 study, has completed, sponsored by Abbott Nutrition.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 168 participants
- Enrollment target
Study Summary
The primary objective of this study is to assess the comparative gastrointestinal (GI) tolerance of normal term infants to two experimental powdered formulas compared with a commercially available powdered formula.
Interventions
- OTHER Hydrolysate based infant formula
- OTHER Investigational Infant Formula A
- OTHER Investigational Infant Formula B
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 168 participants |
| Start Date | 2010-03 |
| Est. Completion | 2010-07 |
| Phase | Phase 3 |
What the finished NCT01155414 record still lists
NCT01155414 is an interventional study that assigns participants to a tested intervention. The registered 168 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (78% lower).
The record links to 0 conditions, and to 3 interventions - of which Hydrolysate based infant formula is the first listed.
NCT01155414 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01155414 about?
NCT01155414 is a clinical study titled "Tolerance of Healthy Term Infants Fed Infant Formulas #4". The primary objective of this study is to assess the comparative gastrointestinal (GI) tolerance of normal term infants to two experimental powdered formulas compared with a commercially available powdered formula.
What is the current status of trial NCT01155414?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 168 participants. The study started on 2010-03. Estimated completion is 2010-07.
What interventions are being tested in trial NCT01155414?
The interventions under investigation include: Hydrolysate based infant formula (OTHER), Investigational Infant Formula A (OTHER), Investigational Infant Formula B (OTHER).
Who is sponsoring clinical trial NCT01155414?
This trial is sponsored by Abbott Nutrition, which has 89 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01155414's enrollment target sits among peer trials
168 1459th of 2000 higher than 538 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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