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NCT01965769 · ClinicalTrials.gov registry record · NA
Effects Of Not Measuring Gastric Residual Content On Feeding Tolerance In Premature Infants iNFANTS
A NA study, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 61
- Enrollment target
NCT01965769: Completed NA study, sponsored by University of Florida.
NCT01965769 is a NA study that has completed, run by University of Florida. The registered enrollment target is 61 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01965769, a NA study, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 61 participants
- Enrollment target
Study Summary
Omitting evaluation of gastric residual contents prior to feeding very premature infants will increase the feeding intake at 2 weeks, and total caloric intake and growth by 3 weeks, as well as decrease the time required for parenteral nutrition.
Interventions
- OTHER No gastric residual evaluation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 61 participants |
| Start Date | 2011-03 |
| Est. Completion | 2013-10 |
| Phase | NA |
What the finished NCT01965769 record still lists
NCT01965769 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 1 intervention - of which No gastric residual evaluation is the first listed.
NCT01965769 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01965769 about?
NCT01965769 is a clinical study titled "Effects Of Not Measuring Gastric Residual Content On Feeding Tolerance In Premature Infants iNFANTS". Omitting evaluation of gastric residual contents prior to feeding very premature infants will increase the feeding intake at 2 weeks, and total caloric intake and growth by 3 weeks, as well as decrease the time required for parenteral nutrition.
What is the current status of trial NCT01965769?
This trial is currently completed. It is a NA study. The enrollment target is 61 participants. The study started on 2011-03. Estimated completion is 2013-10.
What interventions are being tested in trial NCT01965769?
The interventions under investigation include: No gastric residual evaluation (OTHER).
Who is sponsoring clinical trial NCT01965769?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01965769's enrollment target sits among peer trials
61 1164th of 2000 higher than 837 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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