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New oxygen mask could help heart patients breathe easier after surgery

NCT ID NCT06521489

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at a new type of oxygen device (asymmetrical high-flow nasal cannula) for patients recovering from heart surgery. About 63 adults who need extra oxygen after their breathing tube is removed will be randomly assigned to get the new device, a standard high-flow device, or a regular oxygen mask. The goal is to see if the new device helps them avoid needing more intensive breathing support.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

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.

Participants

63 people

The number who actually took part.

Started

May 2024

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: * Cardiac ICU adult patients * \>18 years * After elective or urgent cardiac surgery * Successful Spontaneous Breathing Trial (SBT) with T-piece and FiO2=60%. * pO2/ FiO2 \<150 * Hemodynamically stable (160\>SAP\>90mmHg) Exclusion Criteria: * Obstructive Sleep Apnea Syndrome supported by CPAP mask on ventilator * COPD, officially diagnosed, respiratory failure - on exacerbation with serum blood pH \<7,35. * Patients with tracheostomy, * DNR status, * Glasgow Coma Scale score \< 13, * Insufficient knowledge of the Greek Language * Visual or hearing impairment.

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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

  • Evangelismos General Hospital of Athens

    Athens, Attica, 10676, Greece

More trials for these conditions

Other studies related to the condition(s) this trial covers.