ICU sensor errors may skew critical care decisions
NCT ID NCT07330505
First seen Jun 24, 2026 · Last updated Jul 08, 2026 · Updated 3 times
Summary
This study will check how often the sensors used to measure blood pressure in intensive care patients are not positioned correctly. Such errors can lead to wrong readings and possibly inappropriate treatments. Researchers will observe 60 adult ICU patients on ventilators and vasopressors, recording sensor alignment and any treatment changes over 8 hours.
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 reveal how common sensor misalignment is and help improve accuracy of ICU monitoring, potentially leading to better treatment decisions.
- What could go wrong
- This is a small, early observational study (60 patients) that only measures errors—it does not test any treatment. Results may not apply to all ICUs or change practice directly.
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 60 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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May 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of adult (≥18 years) critically ill, mechanically ventilated ICU patients receiving routine invasive arterial blood pressure and central venous pressure monitoring, often under sedation and vasoactive support.
- 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: * Age ≥18 years * ICU admission * Mechanically ventilated * Arterial catheter for MAP * Central venous catheter for CVP * Ongoing vasopressor therapy Exclusion Criteria: * Severe hemodynamic or respiratory instability * Contraindications for lateral positioning * Expected survival \<24 hours
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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
2 sites. 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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Sahlgrenska University Hospital
RECRUITINGGothenburg, Sweden
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Skaraborgs Sjukhus
NOT_YET_RECRUITINGSkövde, Sweden
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