New device aims to get ICU patients standing sooner
NCT ID NCT05716451
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested a device called Liana that helps critically ill patients on breathing machines sit up and stand. The goal was to see if using the device allows patients to reach a higher level of mobility (like standing) more often during their ICU stay. Forty adult patients in the ICU who needed a ventilator took part. The study also looked at whether the device eases the workload for healthcare staff and improves patients' muscle strength and recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sit/stand stabilizer device (Liana)
- What this could lead to
- If it works, this device could help critically ill patients regain mobility faster and reduce muscle weakness during ICU stays.
- What could go wrong
- This is a small pilot study with only 40 participants, so results may not apply to all ICU patients. The device may not significantly improve outcomes or could be difficult to use in practice.
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
-
40 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Nov 2025
- Lead sponsor
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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
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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 Hide 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: * Intensive care patient with ventilatory support and an expected intensive care stay of at least another 48 h * Age ≥ 18 years * Current length of intensive care stay \< 48 h Exclusion Criteria: * Moribund and critically ill * Suspected 6-month mortality \> 75%. * Increased intracranial pressure * Critically ill after cardiopulmonary resuscitation * Critically ill with primary neuromuscular disease or motor neuron disease * One or more amputated extremities * Patients, within 2h after surgery * Unstable fractures * Severe traumatic brain injury (e.g., brain and skull injuries) * Circulatory instability with norepinephrine \> 0.3 µg/kg/min * Patients for whom there is an indication for deep sedation (RASS -5) * Language barrier * Fitting of legs into leg trays is not possible due to e.g. patient weight
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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
-
Charité - Univiversitätsmedizin Berlin
Berlin, State of Berlin, 10117, Germany
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