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Simple breathing tool may boost oxygen after bypass surgery

NCT ID NCT05192785

Symptom relief Sponsor: Cukurova University Source: ClinicalTrials.gov ↗

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether using an incentive spirometer (a device that encourages deep breathing) after coronary artery bypass surgery helps improve oxygen levels and vital signs. 58 patients were randomly assigned to receive either standard care or standard care plus the breathing device. The researchers measured blood oxygen, carbon dioxide, and blood pressure to see if the device made a difference.

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

58 people

The number who actually took part.

Started

Feb 2021

Finished

Dec 2022

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

Accepted

You do not need to have the condition being studied to take part.

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: * Patients undergoing first-time, nonemergency coronary artery bypass graft surgery * Patients who agreed to participate in the study * Patients who were able to communicate Patients with no hearing difficulty Patients with no history of psychiatric and/or mental illness -Patients with a stable clinical condition Exclusion Criteria: * Patients with an unstable clinical condition * Patients who refused to participate * Patients with chronic obstructive pulmonary disease * Patients with chronic kidney failure * Patients with severe hemodynamic dysfunction * Patients requiring sternotomy or re-sternotomy * Patients requiring prolonged mechanical ventilation

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Conditions

The condition(s) this trial relates to.

coronary artery disorder Coronary Disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Incentive spirometry Oxygen saturation

Contacts and locations

Locations

  • Cukurova University

    Sarıçam, Adana, Turkey (Türkiye)

More trials for these conditions

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