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NCT00609882 · ClinicalTrials.gov registry record · NA
Comparison of Humidified High Flow Nasal Cannula to Nasal CPAP in Neonates
A NA study, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 420
- Enrollment target
NCT00609882: Completed NA study, sponsored by University of Utah.
NCT00609882 is a NA study that has completed, run by University of Utah. The registered enrollment target is 420 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00609882, a NA study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 420 participants
- Enrollment target
Study Summary
We hypothesize that the success rate for keeping babies extubated (without a breathing tube for assisted mechanical ventilation), defined as the proportion of infants remaining extubated for a minimum of 72 hours, will be equivalent among infants managed with nasal CPAP compared to humidified high flow nasal cannula (HHFNC).
Interventions
- OTHER Nasal CPAP
- OTHER Humidified High Flow Nasal Cannula (HHFNC)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 420 participants |
| Start Date | 2007-12 |
| Est. Completion | 2012-06 |
| Phase | NA |
What the finished NCT00609882 record still lists
NCT00609882 is an interventional study that assigns participants to a tested intervention. The registered 420 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower).
The record links to 0 conditions, and to 2 interventions - of which Nasal CPAP is the first listed.
NCT00609882 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00609882 about?
NCT00609882 is a clinical study titled "Comparison of Humidified High Flow Nasal Cannula to Nasal CPAP in Neonates". We hypothesize that the success rate for keeping babies extubated (without a breathing tube for assisted mechanical ventilation), defined as the proportion of infants remaining extubated for a minimum of 72 hours, will be equivalent among infants managed with nasal CPAP compared to humidified high f...
What is the current status of trial NCT00609882?
This trial is currently completed. It is a NA study. The enrollment target is 420 participants. The study started on 2007-12. Estimated completion is 2012-06.
What interventions are being tested in trial NCT00609882?
The interventions under investigation include: Nasal CPAP (OTHER), Humidified High Flow Nasal Cannula (HHFNC) (OTHER).
Who is sponsoring clinical trial NCT00609882?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00609882's enrollment target sits among peer trials
420 239th of 2000 higher than 1,761 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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