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Study to reveal best way to ventilate patients on the move

NCT ID NCT07646249

Knowledge-focused Sponsor: Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Sep 11, 2026 · Updated 2 times

Summary

This study observes 800 adults who need breathing help after major non-cardiac surgery and are moved from the operating room to the ICU. Researchers will compare manual bag ventilation versus portable ventilator use during transport, tracking vital signs and complications. The goal is to identify safer practices for this critical phase of care.

What this could mean

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

What this could lead to
If successful, this study could help identify safer ventilation methods during patient transport, potentially reducing complications.
What could go wrong
This is an observational study, so it cannot prove cause and effect. Results may not apply to all hospitals or patient types.

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.

Participants

About 800 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2026

Expected to finish

Oct 2027

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.

Who is studied

Intubated adult patients (≥18 years) undergoing general anesthesia (intravenous or mixed) for non-cardiac surgery, requiring transport from the operating room to the ICU for continuation/weaning from IMV in the postoperative period.

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 * Intubated patients undergoing general anesthesia for non-cardiac surgery * Requirement for postoperative IMV * Age ≥18 years * Obtained informed consent Exclusion criteria * Patients undergoing cardiac surgery * Patients receiving preoperative mechanical ventilation prior to surgery.

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Conditions

The condition(s) this trial relates to.

Critical Illness Postoperative Complications Respiratory Aspiration

As listed by the trial registrant

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

Critical illness Intensive care units Positive-pressure respiration Postoperative complications Postoperative complications (cardiopulmonary) Respiration, artificial

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Azienda Ospedaliero-Universitaria di Alessandria

    RECRUITING

    Alessandria, Italy, 15121, Italy

More trials for these conditions

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