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NCT Number: NCT05665127

Point of Care Evaluation of High-sensitivity Cardiac Troponin

In this observational research project the investigators wish to test new technologies that could allow them to either detect or rule out heart attacks earlier.

Currently, when a patient attends the Emergency Department with symptoms that could be due to a heart attack, the patient has a blood test taken from a vein in the arm. This is sent to a laboratory to measure the level of a protein called troponin that is released from the heart when it is damaged. Doctors and nurses use the level of troponin measured in that blood sample, along with a tracing of the heart and an assessment of symptoms, to decide whether the patient is having a heart attack. On average, it takes about 2 hours from the patient arriving at hospital to the doctor or nurse receiving the blood test result so they can make this diagnosis.

A device has been designed that can measure troponin by using a drop of blood from a finger prick with the result available in around 10 minutes. This means that if a patient is having a heart attack we can diagnose it earlier and give them treatment. Previous studies have also showed that the majority of patients who attend hospital with chest pain ultimately do not have a heart attack. With this new device the investigators hope to be able to reassure these patients that their symptoms are not due to a heart attack, so the clinical team can concentrate on finding out what else could be causing their chest pain, and ultimately discharge them earlier.

The investigators aim to find the best way to use this new device and look at the impact this device has on the length of time from sample to diagnosis and time spent in hospital.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

NHS Lothian

Edinburgh, United Kingdom

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Type 1, 4b or 4c myocardial infarction or cardiac death

    Time frame: Index presentation to 30 days

Secondary outcomes

  1. Any myocardial infarction

    Time frame: Index presentation to 1 year

  2. Cardiac death

    Time frame: Index presentation to 1 year

  3. Any myocardial infarction or cardiac death

    Time frame: Index presentation to 1 year

  4. Cardiovascular death

    Time frame: Index presentation to 1 year

  5. All-cause death

    Time frame: Index presentation to 1 year

  6. Reattendance with suspected acute coronary syndrome

    Time frame: Index presentation to 1 year

  7. Unplanned coronary revascularization

    Time frame: Following index presentation to 1 year

Other outcomes

  1. Time from presentation to rule-out or rule-in myocardial infarction

    Time frame: Time of index presentation until the time of reporting of the troponin result that rules in or rules out myocardial infarction, assessed up to the end of study follow up (12 months)

  2. Duration of stay in hospital (index)

    Time frame: Time from index presentation until the time of discharge from hospital, assessed up to the end of study follow up (12 months)

  3. Duration of stay in Emergency Department

    Time frame: Time from index presentation until the time of discharge from the Emergency Department, assessed up to the end of study follow up (12 months)

  4. Inter-assay coefficient of variation

    Time frame: During index admission, assessed up to 36 hours following enrolment

Sponsors and collaborators

Lead sponsor

University of Edinburgh

Other

Collaborators

  • British Heart Foundation
  • NHS Grampian
  • Siemens Healthcare Diagnostics Ltd

Registry information

Acronym: POC-ET

Important dates

Study start
2022
Primary completion
2025
Study completion
2027
First posted
Dec 27, 2022
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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