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New lung monitor aims to prevent breathing problems after surgery

NCT ID NCT06899295

Knowledge-focused Sponsor: Assistance Publique - Hôpitaux de Paris 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study watches how the lungs work during surgery in 34 adults under general anesthesia. It uses special monitors to measure lung pressure and air distribution during a routine breathing technique called alveolar recruitment. The goal is to see if these monitors can help doctors set the ventilator more safely and reduce the risk of lung injury after surgery.

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 34 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

May 2028

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

Patients undergoing planned surgery under prolonged general anesthesia (\> 2 hour forecast) * in prone position Or * laparoscopic abdominal surgery Or * Obese patients BMI \> 35

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: 1. Patients ≥ 18 years of age 2. undergoing : * scheduled surgery at Hospital Lariboisière. * scheduled to last more than 2 hours under general anesthesia for abdominal surgery under laparoscopy or surgery in the prone position, or for obese patients with a BMI \>35. * And for whom the ventilator used includes advanced monitoring * for whom placement of a gastric tube is indicated either because of the duration of the procedure or because it is necessary for the surgery. 3. Patient informed and expressing non-opposition to participation in this study Exclusion Criteria: * \- Patients under 18 years of age. * Contraindications to esophageal tube placement * Contraindications to ARMs * Patient opposed to protocol participation * Pregnant, parturient or breast-feeding women * Patient under legal protection

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Conditions

The condition(s) this trial relates to.

Ventilator-Induced Lung Injury

As listed by the trial registrant

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

General anesthesia Postoperative respiratory complications Ventilator-induced lung injuries

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

  • AP-HP, Lariboisière Hospital, Department of Anesthesiology and Intensive Care Paris, France, 75010

    Paris, Île-de-France Region, 75010, France

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