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Sleep monitoring in the ICU could cut breathing tube use by half

NCT ID NCT07606495

Symptom relief Sponsor: Poitiers University Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 21, 2026 · Updated 1 time

Summary

This study tests whether improving sleep in intensive care unit (ICU) patients can help them recover better. Researchers will use a sleep monitor to guide nurses in postponing non-urgent care when patients are asleep. The goal is to see if this approach reduces the need for breathing machines or death within 7 days. About 460 conscious ICU patients will take part.

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 460 people

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

Started

Sep 2026

Expected to finish

Jun 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.

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: * Patients aged 18 years or older admitted to an intensive care unit * Conscious patients with a Richmond Agitation-Sedation Scale (RASS) score between -2 and +1 * Patients without continuous sedation, regardless of ventilatory support * No indication for urgent intubation (\<12 hours) * Informed consent from the relatives or the patient himself Exclusion Criteria: * Brain tumor or neuropsychiatric disorders affecting sleep * Amission for stroke or epilepsy * Administration of sleep-modifying medication within 24 hours prior to randomization * Patients with skin lesions around the central right and left areas preclunding the placement of the electrodes * Patients with expected ICU length of stay less than 48 hours * Patients with limitation or withdrawal of life-sustaining therapies * Patients already included in the study during a previous hospitalization * Patients under law protection (guardianship, conservatorship, or judicial protective measures) * People under protection (minors, persons deprived of liberty by a judicial or administrative decision, patients in emergency situations)

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Conditions

The condition(s) this trial relates to.

sleep disorder

As listed by the trial registrant

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

Intensive care unit (ICU) Sleep disruption Sleep monitoring

How to take part

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

  1. The places running it

    7 sites. 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

  • La Rochelle Hospital

    NOT_YET_RECRUITING

    La Rochelle, France

  • Le Mans Hospital

    NOT_YET_RECRUITING

    Le Mans, France

  • Poitiers University Hospital

    RECRUITING

    Poitiers, France

  • Rennes University Hospital

    NOT_YET_RECRUITING

    Rennes, France

  • Saintes Hospital

    NOT_YET_RECRUITING

    Saintes, France

  • Tours University Hospital

    NOT_YET_RECRUITING

    Tours, France

  • Vendée Hospital

    NOT_YET_RECRUITING

    La Roche-sur-Yon, France

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