Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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 is a NA study that has completed, run by University of Florida. The registered enrollment target is 61 participants.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01965769
The ClinicalTrials.gov registry entry for NCT01965769 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which No gastric residual evaluation is the first listed.
NCT01965769 reports 0 study locations.
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
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
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.