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NCT01787019 · ClinicalTrials.gov registry record · Phase 2
Initiation of Oral Feeding at 30 Versus 33 Weeks Postmenstrual Age
A Phase 2 study of Prematurity, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- Phase 2
- Development phase
- 66
- Enrollment target
- 1
- Study location
NCT01787019 is a Phase 2 study of Prematurity that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 66 participants, below the 208-participant average among 21 other Prematurity trials with a reported enrollment target (68% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01787019, a Phase 2 study of Prematurity, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 66 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of the study is to determine if earlier initiation of oral (by mouth as opposed to tube) feedings in premature infants results in earlier attainment of full oral feedings and/or discharge.
Conditions Studied
Interventions
- OTHER Oral feeding
Study Locations (1)
Texas
- Children's Memorial Hermann Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2013-01 |
| Est. Completion | 2016-04 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01787019
The ClinicalTrials.gov registry entry for NCT01787019 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 208-participant average among 21 other Prematurity trials with a reported enrollment target (68% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Prematurity appearing as the primary indexed condition, and to 1 intervention - of which Oral feeding is the first listed.
NCT01787019 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT01787019 about?
NCT01787019 is a clinical study titled "Initiation of Oral Feeding at 30 Versus 33 Weeks Postmenstrual Age". The purpose of the study is to determine if earlier initiation of oral (by mouth as opposed to tube) feedings in premature infants results in earlier attainment of full oral feedings and/or discharge.
What is the current status of trial NCT01787019?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 66 participants. The study started on 2013-01. Estimated completion is 2016-04.
What conditions does trial NCT01787019 study?
This clinical trial studies the following conditions: Prematurity.
What interventions are being tested in trial NCT01787019?
The interventions under investigation include: Oral feeding (OTHER).
Who is sponsoring clinical trial NCT01787019?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01787019 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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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.