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NCT01420263 · ClinicalTrials.gov registry record · NA
Re-feeding Gastric Residuals in Preterm Infants
A NA study, sponsored by University of Alabama at Birmingham.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
NCT01420263 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 72 participants.
The verdict
NCT01420263, a NA study, has completed, sponsored by University of Alabama at Birmingham.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether re-feeding of gastric residuals reduces the time needed to establish full enteral feedings in premature infants. Infants with gestational ages 23-28 weeks at birth will be randomized within one week to receive either gastric residuals or fresh formula or breastmilk whenever significant residuals during feeding advancement require clinical assessment for continuing feedings. Primary outcome measure is time to establish full enteral feedings (120cc/kg/day).
Interventions
- PROCEDURE Re-feeding residuals
- PROCEDURE Fresh Feeding Breastmilk or Formula only
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2011-08 |
| Est. Completion | 2013-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01420263
The ClinicalTrials.gov registry entry for NCT01420263 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Re-feeding residuals is the first listed.
NCT01420263 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01420263 about?
NCT01420263 is a clinical study titled "Re-feeding Gastric Residuals in Preterm Infants". The purpose of this study is to determine whether re-feeding of gastric residuals reduces the time needed to establish full enteral feedings in premature infants. Infants with gestational ages 23-28 weeks at birth will be randomized within one week to receive either gastric residuals or fresh formul...
What is the current status of trial NCT01420263?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2011-08. Estimated completion is 2013-01.
What interventions are being tested in trial NCT01420263?
The interventions under investigation include: Re-feeding residuals (PROCEDURE), Fresh Feeding Breastmilk or Formula only (PROCEDURE).
Who is sponsoring clinical trial NCT01420263?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
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