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NCT05880836 · ClinicalTrials.gov registry record · NA

In Line Aerosol Nebulization With High Flow

A NA study, sponsored by University of California, Los Angeles.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT05880836: Completed NA study, sponsored by University of California, Los Angeles.

NCT05880836 is a NA study that has completed, run by University of California, Los Angeles. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05880836, a NA study, has completed, sponsored by University of California, Los Angeles.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The objective of ILAN is to assess the safety, feasibility and bronchodilator efficacy of in-line bronchodilator nebulizer delivery with VMN via HFNC system in hypoxemic respiratory failure patients treated with bronchodilators and compare this method to standard-nebulization using a jet nebulizer with a facial mask. The investigators hypothesized that aerosol nebulization using HFNC/VMN represents safer and more convenient approach in hypoxemic respiratory failure patients in comparison to conventional therapy while providing similar bronchodilator efficacy.

Primary Outcome

Primary Outcome

Interventions

  • DEVICE nebulizer via in-line drug delivery maintaining high-flow nasal cannula oxygen
  • DEVICE standard jet nebulization (SJN) with face mask

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-09-01
Est. Completion 2025-01-01
Phase NA

What the finished NCT05880836 record still lists

NCT05880836 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which nebulizer via in-line drug delivery maintaining high-flow nasal cannula oxygen is the first listed.

NCT05880836 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05880836 about?

NCT05880836 is a clinical study titled "In Line Aerosol Nebulization With High Flow". The objective of ILAN is to assess the safety, feasibility and bronchodilator efficacy of in-line bronchodilator nebulizer delivery with VMN via HFNC system in hypoxemic respiratory failure patients treated with bronchodilators and compare this method to standard-nebulization using a jet nebulizer w...

What is the current status of trial NCT05880836?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2023-09-01. Estimated completion is 2025-01-01.

What interventions are being tested in trial NCT05880836?

The interventions under investigation include: nebulizer via in-line drug delivery maintaining high-flow nasal cannula oxygen (DEVICE), standard jet nebulization (SJN) with face mask (DEVICE).

Who is sponsoring clinical trial NCT05880836?

This trial is sponsored by University of California, Los Angeles, which has 897 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05880836's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 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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Source: ClinicalTrials.gov NCT05880836, the US trial registry maintained by the National Library of Medicine. NCT05880836 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.