New scale could help prevent bedsores in intensive care
NCT ID NCT07575581
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a Spanish pressure injury risk scale, called EVARUCI, works well in Turkish intensive care units. Researchers translated it and checked its accuracy in 100 adult ICU patients without existing bedsores. The goal was to give nurses a reliable way to spot patients at risk and prevent painful pressure injuries.
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 could give Turkish ICU nurses a reliable tool to better predict and prevent pressure injuries in critically ill patients.
- What could go wrong
- This is a small, completed validation study (100 patients) in a single country. The scale may not work as well in other settings or populations.
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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100 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Feb 2026
- 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 patient
- Ages
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18 to 70 years
- 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 who are 18 years or older * without a pressure injury at the time of ICU admission * expected to stay in the ICU for at least 72 hours who consent to participate in the study (or whose family members consent) included in the study. Exclusion Criteria: * Patients or their family members who did not consent to participate * Patients who transferred to another hospital during their ICU stay, excluded from the study.
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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
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Istanbul University
Istanbul, Turkey (Türkiye)