10-Minute Finger-Prick test could revolutionize heart attack diagnosis
NCT ID NCT05665127
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study is testing a new finger-prick blood test that measures troponin levels in about 10 minutes, compared to the usual 2-hour lab test. Researchers hope it will help diagnose heart attacks faster and reassure patients who are not having one, allowing them to be discharged sooner. The study involves 1,000 adults coming to the emergency department with symptoms of a possible heart attack.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- finger-prick high-sensitivity troponin test
- What this could lead to
- If successful, this could allow doctors to diagnose or rule out heart attacks in minutes instead of hours, leading to faster treatment and earlier discharge.
- What could go wrong
- This is an observational study, not a treatment trial. The test may not be accurate enough in real-world settings, and results may not change patient outcomes as hoped.
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
-
About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Nov 2022
- Expected to finish
-
Feb 2027
An estimate. End dates often move.
- Lead sponsor
-
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
Patients with suspected acute coronary syndrome attending the Emergency Department or Acute Medical Unit
- Ages
-
18 years and older
- Sex
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Anyone
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: * Presenting to hospital with symptoms of suspected acute coronary syndrome * Age 18 years and over Exclusion Criteria: * Patients with ST-segment elevation on the electrocardiogram * Patients presenting with an out-of-hospital cardiac arrest * Patients unable or unwilling to give informed consent * Patients unable or unwilling to comply with study protocol * Previous enrolment in this 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
-
NHS Lothian
Edinburgh, United Kingdom
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Other studies related to the condition(s) this trial covers.
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