Asthma oxygen study pulled before it started
NCT ID NCT06379607
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to compare standard oxygen therapy with two different flow rates of high-flow nasal cannula in children aged 2-17 with moderate to severe asthma. The goal was to see if it was possible to enroll enough patients and measure breathing improvements. However, the study was withdrawn before any participants were enrolled, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
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Jan 2025
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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2 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 2-17 years old with prior clinical diagnosis of asthma * Admitted to PICU on standard asthma therapy defined as continuous albuterol and systemic corticosteroids * Admitted to PICU on either COT or HFNC * Admitted to PICU from either Golisano Children's Hospital ED or as a transport from an outside hospital ED within 6 hours of initial presentation * PRAM score greater than or equal to 4 after completion of initial ED therapy Exclusion Criteria: * Admitted to the PICU on NIV or invasive mechanical ventilation * Admitted to the PICU from general floors or \> 6 hours from initial presentation * Presence of a tracheostomy or baseline NIV requirement * Pregnancy * Immunocompromised State
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Rochester Golisano Children's Hospital
Rochester, New York, 14642, United States
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University of Rochester Medical Center
Rochester, New York, 14642, United States
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Other studies related to the condition(s) this trial covers.
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