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Pilot study tests best way to manage sedation for ventilator patients

NCT ID NCT02219659

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested three different ways to manage pain and sedation in 90 adults on breathing machines (mechanical ventilation) for at least 48 hours. The goal was to see which approach was most practical and how it affected time in the ICU. The study did not aim to cure or treat a disease, but to gather knowledge on improving care for patients with acute respiratory failure.

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

90 people

The number who actually took part.

Start date

Dec 2014

Finished

May 2018

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: 1. ≥ 18 years of age 2. Mechanically ventilated with an expected duration of MV ≥ 48 hours 3. ICU team has initiated continuous sedative and/or /analgesic infusions Exclusion criteria: 1. Admission after resuscitation from cardiac arrest 2. Admission with traumatic brain injury or another acute neurologic event (e,g. stroke, uncontrolled seizures). 3. History of severe dementia 4. Admission because of acute alcohol withdrawal or acute drug intoxication 5. Administration of more than 24 hours of continuous sedation 6. Allergy to fentanyl, midazolam, and/or propofol 7. Lack of informed consent

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Long Beach Memorial Medical Center

    Long Beach, California, 90806, United States

More trials for these conditions

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