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NCT01220687 · ClinicalTrials.gov registry record · NA
Inhaled Nitric Oxide (iNO) as an Adjunct to Neonatal Resuscitation
A NA study of Very Low Birth Weight Baby and Respiratory Distress Syndrome in Premature Infants, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 33
- Enrollment target
- 2
- Study locations
NCT01220687 is a NA study of Very Low Birth Weight Baby and Respiratory Distress Syndrome in Premature Infants that has completed, run by University of Oklahoma. The registered enrollment target is 33 participants. The trial reports 2 study locations across 1 state.
The verdict
NCT01220687, a NA study of Very Low Birth Weight Baby and Respiratory Distress Syndrome in Premature Infants, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 33 participants
- Enrollment target
- 2
- Study locations
Study Summary
This study hopes to determine whether nitric oxide along with oxygen during the first 20 minutes of life in infants needing help with breathing will reduce the percentage and total exposure to oxygen during that time frame. Although the use of oxygen in management of breathing is an important part of supporting baby immediately after delivery, there is more evidence that too much exposure to oxygen may lead to potential problems for your baby later. Oxygen exposure can be harmful to premature babies developing lungs.
Conditions Studied
Interventions
- DRUG iNO
- OTHER Nitrogen
Study Locations (2)
Oklahoma
- University of Oklahoma Health Sciences Center - Oklahoma City
- University of Oklahoma, Childrens Hospital - Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2011-04 |
| Est. Completion | 2017-05-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01220687
The ClinicalTrials.gov registry entry for NCT01220687 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Very Low Birth Weight Baby appearing as the primary indexed condition, and to 2 interventions - of which iNO is the first listed.
NCT01220687 reports 2 study locations spanning 1 distinct geographic area - top geographies include Oklahoma.
Frequently Asked Questions
What is clinical trial NCT01220687 about?
NCT01220687 is a clinical study titled "Inhaled Nitric Oxide (iNO) as an Adjunct to Neonatal Resuscitation". This study hopes to determine whether nitric oxide along with oxygen during the first 20 minutes of life in infants needing help with breathing will reduce the percentage and total exposure to oxygen during that time frame. Although the use of oxygen in management of breathing is an important part o...
What is the current status of trial NCT01220687?
This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2011-04. Estimated completion is 2017-05-01.
What conditions does trial NCT01220687 study?
This clinical trial studies the following conditions: Very Low Birth Weight Baby, Respiratory Distress Syndrome in Premature Infants.
What interventions are being tested in trial NCT01220687?
The interventions under investigation include: iNO (DRUG), Nitrogen (OTHER).
Who is sponsoring clinical trial NCT01220687?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01220687 being conducted?
This trial has 2 study locations across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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