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Massive study tracks hidden toll of ICU stays
NCT ID NCT07290712
First seen Jun 27, 2026 · Last updated Aug 26, 2026 · Updated 2 times
Summary
This study follows 5,000 patients who spent more than 72 hours in the ICU to understand long-term cognitive, physical, and emotional problems known as Post-Intensive Care Syndrome (PICS). Researchers will collect data during the hospital stay and for up to five years after discharge, using questionnaires and blood samples. The goal is to identify risk factors and improve care for patients and their families.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could identify risk factors and better ways to diagnose and treat long-term problems after intensive care.
- What could go wrong
- This is an observational registry, not a treatment trial. It will not test any new drug or therapy, so direct patient benefits may take years to emerge.
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
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About 5,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Nov 2035
An estimate. End dates often move.
- 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.
Who is studied
Intensive care unit patients
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Patients with an ICU stay longer than 72 hours will be included Exclusion Criteria: * Age \< 18 years old * Patients who receive end-of-life care at the time of screening
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Charité - Universitätsmedizin Berlin
RECRUITINGBerlin, State of Berlin, 13353, Germany
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Medical University of Vienna
RECRUITINGVienna, State of Vienna, 1090, Austria
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Universitätsklinikum Augsburg
RECRUITINGAugsburg, Bavaria, 86156, Germany
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Universitätsklinikum Würzburg
NOT_YET_RECRUITINGWürzburg, Bavaria, 97080, Germany
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