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Which breathing method is safer for heart surgery patients on the move?

NCT ID NCT06006208

Knowledge-focused Sponsor: Thomas Jefferson 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study looked at 78 adults who had heart surgery and needed a breathing tube while being moved to the intensive care unit. Researchers compared using a manual bag (AMBU bag) versus a mechanical ventilator (Hamilton C1) to see which method kept blood pressure and oxygen levels more stable. The goal is to find the safest way to transport these patients.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Hamilton C1 ventilator
What this could lead to
If it works, this could help hospitals choose the best way to keep patients stable during transport after heart surgery.
What could go wrong
This is a small, completed study with only 78 participants, so results may not apply to all patients or hospitals. It compares two methods but does not test a new treatment.

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

78 people

The number who actually took part.

Started

Nov 2023

Finished

Apr 2025

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: * Over 18 years old (any gender or race) * Cardiac surgery * Require postoperative mechanical ventilation and care in the ICU. Exclusion Criteria: * Patients' refusal * Extubation in OR * On mechanical circulatory support * Requirement for postoperative therapy with inhaled pulmonary vasodilators (epoprostenol (FLOLAN), inhaled nitric oxide, etc.) * Severe RV dysfunction with preoperative echocardiography * Contraindication to TEE and pulmonary artery catheter.

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Conditions

The condition(s) this trial relates to.

postoperative ventricular dysfunction

As listed by the trial registrant

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

Cardiac function disturbance postoperative Manual ventilation Mechanical ventilation Oxygenation Point-of-care ultrasound

Contacts and locations

Locations

  • Thomas Jefferson University

    Philadelphia, Pennsylvania, 19107, United States

More trials for these conditions

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