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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04087538
Other study ID # 19000557
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2021
Est. completion date April 1, 2024

Study information

Verified date June 2023
Source Herlev Hospital
Contact Kasper Iversen, Dmsc
Phone 28712753
Email Kasper.karmark.iversen@regionh.dk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The rising number of patients with chest pain without myocardial infarction has made accurate diagnosis important. Unnecessary invasive coronary angiographies are increasingly prevalent. These are both costly and lead to rare but serious adverse events. Recent studies suggest cardiac Troponin I is more cardiac specific than cardiac Troponin T. In this study we will investigate whether using cardiac Troponin I lead to fewer unnecessary procedures in clinical practice (i.e. invasive coronary angiography and non-invasive tests)


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date April 1, 2024
Est. primary completion date October 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Admitted to either Herlev-Gentofte or Amager-Hvidovre Hospital - Clinically suspected of NSTEMI - Referred to invasive coronary angiography (ICA) - Recieved at least one measurement of either troponin Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Troponin T and I
Does the use of troponin T or I increase the number of patients referred to coronary angiography

Locations

Country Name City State
Denmark Bispebjerg Hospital Bispebjerg Copenhagen
Denmark Herlev-Gentofte Hospital Herlev

Sponsors (1)

Lead Sponsor Collaborator
Herlev Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Specificity for MI The difference in specificity of cardiac Troponin and I in detecting patients with significant CAD. The specificity will be defined as the proportion of patients with no significant CAD on ICA correctly identified as low-risk patients and not referred to ICA upon the review by the senior cardiologists 0
Primary Cost-effectiveness The cost-effectiveness of using cardiac Troponin T compared to cardiac Troponin I. This will be defined by the number of patients sent to ICA and the associated costs of this. 0
Secondary Sensitivity for MI A safety outcome of difference in sensitivity of cardiac Troponin T and cardiac Troponin I in the detection of patients with significant coronary artery disease. The sensitivity is defined as the proportion of patients with significant coronary artery disease that were referred to ICA upon review by the senior cardiologists 0
Secondary Elevated troponin without CAD The difference in the proportion of patients with elevated cardiac Troponin T or cardiac Troponin I above the 99th percentile with no significant CAD on ICA 0
Secondary Number of MIs The difference in the number of patients diagnosed with MI for each cardiac Troponin 0
Secondary PPV and NPV The difference in positive predictive value and negative predictive value of each cardiac Troponin 0
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