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NCT01270581 · ClinicalTrials.gov registry record · NA
High Flow Nasal Cannula Versus Bubble Nasal CPAP for the Treatment of Transient Tachypnea of the Newborn in Infants ≥ 35 Weeks Gestation
A NA study, sponsored by Icahn School of Medicine at Mount Sinai.
- Terminated
- Registry status
- NA
- Development phase
- 7
- Enrollment target
NCT01270581: Clinical Trial NA study, sponsored by Icahn School of Medicine at Mount Sinai.
NCT01270581 is a NA study that was terminated before completion, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01270581, a NA study, was terminated before completion, sponsored by Icahn School of Medicine at Mount Sinai.
- TERMINATED
- Registry status
- NA
- Development phase
- 7 participants
- Enrollment target
Study Summary
The primary objective is to determine whether High Flow Nasal Cannula (HFNC) is a superior respiratory modality for neonates ≥36 weeks with transient tachypnea of the newborn (TTN) when compared to the standard of care modality (NCPAP).
Primary Outcome
Data not collected due to insufficient enrollment for any data analysis.
Interventions
- OTHER High Flow Nasal Cannula
- OTHER Bubble Nasal CPAP
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2010-07 |
| Est. Completion | 2012-04 |
| Phase | NA |
Why NCT01270581 stopped before completion
NCT01270581 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which High Flow Nasal Cannula is the first listed.
NCT01270581 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01270581 about?
NCT01270581 is a clinical study titled "High Flow Nasal Cannula Versus Bubble Nasal CPAP for the Treatment of Transient Tachypnea of the Newborn in Infants ≥ 35 Weeks Gestation". The primary objective is to determine whether High Flow Nasal Cannula (HFNC) is a superior respiratory modality for neonates ≥36 weeks with transient tachypnea of the newborn (TTN) when compared to the standard of care modality (NCPAP).
What is the current status of trial NCT01270581?
This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2010-07. Estimated completion is 2012-04.
What interventions are being tested in trial NCT01270581?
The interventions under investigation include: High Flow Nasal Cannula (OTHER), Bubble Nasal CPAP (OTHER).
Who is sponsoring clinical trial NCT01270581?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01270581's enrollment target sits among peer trials
7 1982nd of 2000 higher than 18 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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