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NCT04258020 · ClinicalTrials.gov registry record · NA

Postextubation Management in Patients at Risk for Extubation Failure

A NA study, sponsored by OhioHealth.

Terminated
Registry status
NA
Development phase
6
Enrollment target

NCT04258020: Clinical Trial NA study, sponsored by OhioHealth.

NCT04258020 is a NA study that was terminated before completion, run by OhioHealth. The registered enrollment target is 6 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.

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The verdict

NCT04258020, a NA study, was terminated before completion, sponsored by OhioHealth.

TERMINATED
Registry status
NA
Development phase
6 participants
Enrollment target

Study Summary

At the time of weaning from mechanical ventilation, patients with heart and/or lung conditions will be given oxygen support with alternating bilevel positive airway pressure (BiPAP; oxygen via face mask) and heated high flow nasal cannula oxygen (HFNC; oxygen via nasal cannula) to see if this method reduces the likelihood of re-intubation.

Primary Outcome

The number of patients who require re-intubation

Interventions

  • DEVICE HFNC
  • DEVICE BiPAP

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2020-02-11
Est. Completion 2020-04-02
Phase NA
OhioHealth

20 total trials

Why NCT04258020 stopped before completion

NCT04258020 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 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 HFNC is the first listed.

NCT04258020 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04258020 about?

NCT04258020 is a clinical study titled "Postextubation Management in Patients at Risk for Extubation Failure". At the time of weaning from mechanical ventilation, patients with heart and/or lung conditions will be given oxygen support with alternating bilevel positive airway pressure (BiPAP; oxygen via face mask) and heated high flow nasal cannula oxygen (HFNC; oxygen via nasal cannula) to see if this method...

What is the current status of trial NCT04258020?

This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2020-02-11. Estimated completion is 2020-04-02.

What interventions are being tested in trial NCT04258020?

The interventions under investigation include: HFNC (DEVICE), BiPAP (DEVICE).

Who is sponsoring clinical trial NCT04258020?

This trial is sponsored by OhioHealth, which has 20 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04258020's enrollment target sits among peer trials

6 1983rd of 2000 higher than 13 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 NCT04258020, the US trial registry maintained by the National Library of Medicine. NCT04258020 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.