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New monitoring method may shorten time on breathing machines after major surgery

NCT ID NCT07339449

Knowledge-focused Sponsor: University Hospital Dubrava 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether using extra monitoring devices during major abdominal surgery can help high-risk patients (aged 50 and older) spend less time on a breathing machine afterward. One group will receive standard care, while the other will have additional sensors and a special drug plan. The goal is to see if this approach leads to faster recovery and fewer complications.

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

About 100 people

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

Started

Aug 2025

Expected to finish

Jun 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.

Ages

50 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: * aged 50 years or older * scheduled for elective major abdominal surgery, specifically those classified as ASA II and ASA III Exclusion Criteria: * patient refusal; * memory impairment (psychosis); * known or suspected electroencephalo-graphic abnormalities (such as epilepsy or previous brain surgery); * chronic use of psy-choactive medication; * urgent or emergent procedures; * body mass index (BMI) below 18 kg/m2 or above 35 kg/m2; * persistent arrhythmias including atrial fibrillation and undulation; * documented NYHA class III-IV heart failure or a preoperative left ventricular ejection fraction below 30%; * valvular disease involving aortic and/or mitral stenosis or regurgita-tion; * liver diseases such as decompensated cirrhosis and coagulopathies; * anticipated operation duration exceeding six hours.

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As listed by the trial registrant

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

Major abdominal surgeries Mechanical ventilation

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

  • University hospital Dubrava

    RECRUITING

    Zagreb, Croatia, 10040, Croatia

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