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NCT03120585 · ClinicalTrials.gov registry record · NA
Fluid Restriction in Respiratory Distress of the Newborn
A NA study of Respiratory Distress Syndrome, Newborn, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 65
- Enrollment target
- 2
- Study locations
NCT03120585 is a NA study of Respiratory Distress Syndrome, Newborn that has completed, run by University of Oklahoma. The registered enrollment target is 65 participants, below the 200-participant average among 8 other Respiratory Distress Syndrome, Newborn trials with a reported enrollment target (67% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT03120585, a NA study of Respiratory Distress Syndrome, Newborn, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 65 participants
- Enrollment target
- 2
- Study locations
Study Summary
The object of this study is to determine the best way to care for infants with respiratory distress. The investigators are testing a method of feeding fluids to infants with respiratory distress in amounts similar to what healthy breastfed babies eat when they are feeding on demand, and comparing this method to the current standard of care for feeding fluids to infants with respiratory distress. These methods of feeding fluids to the study infants will continue until the infants are able to feed normally by mouth. The study will include about 400 infants across five sites in the United States, Chile and Argentina.
Conditions Studied
Interventions
- OTHER Fluid Management Intervention
Study Locations (2)
New York
- Icahn School of Medicine at Mount Sinai - New York
Oklahoma
- Comanche county Memorial hospital - Lawton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2017-03-01 |
| Est. Completion | 2021-03-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03120585
The ClinicalTrials.gov registry entry for NCT03120585 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 200-participant average among 8 other Respiratory Distress Syndrome, Newborn trials with a reported enrollment target (67% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Respiratory Distress Syndrome, Newborn appearing as the primary indexed condition, and to 1 intervention - of which Fluid Management Intervention is the first listed.
NCT03120585 reports 2 study locations spanning 2 distinct geographic areas - top geographies include New York, Oklahoma.
Frequently Asked Questions
What is clinical trial NCT03120585 about?
NCT03120585 is a clinical study titled "Fluid Restriction in Respiratory Distress of the Newborn". The object of this study is to determine the best way to care for infants with respiratory distress. The investigators are testing a method of feeding fluids to infants with respiratory distress in amounts similar to what healthy breastfed babies eat when they are feeding on demand, and comparing th...
What is the current status of trial NCT03120585?
This trial is currently completed. It is a NA study. The enrollment target is 65 participants. The study started on 2017-03-01. Estimated completion is 2021-03-31.
What conditions does trial NCT03120585 study?
This clinical trial studies the following conditions: Respiratory Distress Syndrome, Newborn.
What interventions are being tested in trial NCT03120585?
The interventions under investigation include: Fluid Management Intervention (OTHER).
Who is sponsoring clinical trial NCT03120585?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03120585 being conducted?
This trial has 2 study locations across New York, Oklahoma. 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
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