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Ultrasound may predict lung risk after surgery

NCT ID NCT03289975

Knowledge-focused Sponsor: Centre Hospitalier Universitaire Dijon 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 165 patients in the intensive care unit after major abdominal or urinary surgery. Doctors used lung ultrasound to measure fluid in the lungs and see if it could predict who would develop severe breathing problems. The goal was to find a simple bedside test to catch trouble early.

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

165 people

The number who actually took part.

Started

Mar 2016

Finished

Mar 2017

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 digestive or urinary surgery and requiring post-operative intensive care

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: All patients undergoing scheduled or emergency visceral surgery and admitted to an ICU following the intervention. Exclusion Criteria: * Chest surgery * ASA (American Society of Anesthesiologists) 4 or more * Refusal of the patient * Pregnant women * Spontaneously-breathing patients

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As listed by the trial registrant

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

Digestive surgery Urinary surgery

Contacts and locations

Locations

  • Chu Dijon Bourogne

    Dijon, France