Silent suffering: new study tracks pain in comatose cardiac arrest patients
NCT ID NCT07564778
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how much pain people feel after a cardiac arrest while they are in the intensive care unit. Researchers will track pain using special scales, even in patients who are unconscious or on a breathing machine. The goal is to understand how pain affects recovery, such as time on a ventilator or in the ICU. About 300 adults who had a cardiac arrest outside the hospital and are still unconscious will take part.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Oct 2028
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
STEPCARE participants at PAINCARE-participating sites who are included under approved PAINCARE substudy procedures and have not withdrawn consent for use of study data according to parent-trial procedures. PAINCARE participants may be included retrospectively or prospectively according to local approvals and substudy implementation.
- 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: * Out-of-hospital cardiac arrest * Adult, age 18 years or older * Spontaneous circulation without chest compressions for at least 20 minutes * Comatose, defined as not obeying verbal commands * Enrolled within 4 hours after return of spontaneous circulation Exclusion Criteria: * Restrictions or limitations of care * On extracorporeal membrane oxygenation before randomization * Pregnancy * Previously randomized in the STEPCARE trial * Trauma or hemorrhage as the presumed cause of arrest * Suspected or confirmed intracranial hemorrhage
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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
3 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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Dep. of Intensive Care Halmstad Lasarett
RECRUITINGHalmstad, Sweden
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Dep. of Intensive Care, Norrlands Universitets Sjukhus
RECRUITINGUmeå, Sweden
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Department of Intensive Care, Skåne University Hospital
RECRUITINGMalmö, 20205, Sweden
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Other studies related to the condition(s) this trial covers.
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- Mean arterial pressure after out-of-hospital cardiac arrest: the METAPHORE randomized trial
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