ACTIVE_NOT_RECRUITING

Emergency Department Triage of Patients With Acute Chest Pain Based on the ESC 0/1-hour Algorithm (PRESC1SE-MI)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The PRESC1SE-MI study compares two algorithms for triage of patients presenting with chest pain and symptoms of heart attack (myocardial infarction) to the emergency department. Both algorithms are recommended by the European Society of Cardiology: the 0/3-hour algorithm and the 0/1-hour algorithm. Currently, most emergency departments worldwide use the 0/3-hour troponin algorithm. Cardiac troponin (cTn) is a heart-specific biomarker which indicates damage of the heart muscle and which increases after a heart attack. In the 0/3-hour algorithm, the amount of troponin in the bloodstream is measured with a high-sensitivity assay at admission and 3 hours thereafter. Likewise, the 0/1-hour algorithm means that the blood sample in which the troponin is measured is collected at admission and 1 hour later. Since recent clinical studies suggest that the 0/1-hour algorithm is superior to the 0/3-hour algorithm, many hospitals consider switching to the 0/1-hour algorithm. The aim of this study is to assess how feasible the time-saving 0/1-hour algorithm would be in reality and whether it provides the same accuracy and safety in the diagnosis of myocardial infarction as the current practice the 0/3-hour algorithm.

Official Title

PRospective Evaluation of the European Society of Cardiology 0/1-hour Algorithm's Safety and Efficacy for Triage of Patients With Suspected Myocardial Infarction (PRESC1SE-MI)

Quick Facts

Study Start:2020-12-01
Study Completion:2026-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05649384

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients aged 18 and above
  2. * Presentation with acute non-traumatic acute chest pain to the emergency department
  3. * Suspicion of acute myocardial infarction
  1. * Terminal kidney failure requiring dialysis
  2. * Cardiac arrest
  3. * Cardiogenic shock

Contacts and Locations

Principal Investigator

Christian Müller, MD Prof.
PRINCIPAL_INVESTIGATOR
University Hospital, Basel, Switzerland
Jasper Boeddinghaus, MD
PRINCIPAL_INVESTIGATOR
University Hospital, Basel, Switzerland

Study Locations (Sites)

Baylor St. Luke's Medical Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: University Hospital, Basel, Switzerland

  • Christian Müller, MD Prof., PRINCIPAL_INVESTIGATOR, University Hospital, Basel, Switzerland
  • Jasper Boeddinghaus, MD, PRINCIPAL_INVESTIGATOR, University Hospital, Basel, Switzerland

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-12-01
Study Completion Date2026-05-31

Study Record Updates

Study Start Date2020-12-01
Study Completion Date2026-05-31

Terms related to this study

Keywords Provided by Researchers

  • ESC 0/1-hour algorithm
  • Emergency department
  • Chest pain
  • Chest discomfort
  • Myocardial Infarction MI
  • Acute Myocardial Infarction AMI
  • Acute Coronary Syndrome ACS
  • NSTEMI Non-ST-segment elevation myocardial infarction
  • NSTE-ACS Non-ST-segment elevation acute coronary syndrome
  • Unstable angina
  • Damaged muscle of the heart
  • Cardiac Biomarkers
  • Cardiac Troponin T cTnT
  • Cardiac-Specific Troponin T
  • Cardiac Troponin I cTnI
  • Cardiac-Specific troponin I
  • Amount of troponin in the bloodstream
  • Increased troponin level
  • Elevated troponin level
  • High troponin level
  • Troponin assessment
  • Measurement of troponin levels
  • High-sensitive troponin test
  • High-sensitivity troponin T testing
  • High-sensitive Troponin T hsTnT
  • cTnT-hs
  • High-sensitive Troponin I hsTnI
  • cTnI-hs
  • High-sensitivity cardiac troponin assays
  • ED presentation
  • ED admission
  • ED work-up
  • Triage emergency department
  • Triage emergency room
  • Triage emergency hospital
  • Rapid Rule-out of Acute Myocardial Infarction
  • Shorter stay in the emergency department
  • ESC 0/3-hour algorithm
  • ESC Guidelines
  • European Guidelines
  • 0/1-hour algorithm
  • 0/3-hour algorithm

Additional Relevant MeSH Terms

  • Acute Chest Pain
  • NSTEMI - Non-ST Segment Elevation MI