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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03137550
Other study ID # PV4023
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 12, 2017
Est. completion date April 30, 2022

Study information

Verified date May 2022
Source Universitätsklinikum Hamburg-Eppendorf
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Main aim of the COMBAT-CAD-Study is to clarify, if the combination of stress testing with biomarkers improves the diagnostic accuracy. Hypothesis of our study is that diagnosis of CAD can be improved by adding biomarkers to solely stress testing for the workup of patients with suspected CAD or progress of already known CAD.


Description:

The COMBAT-CAD Study is an observational study with the aim to improve the diagnostic accuracy by a combination of stress testing with sensitive and specific biomarkers in detecting coronary artery disease or its progress. The main subjects are all patients with CAD or suspicion of CAD sent to the University Heart Center Hamburg. In these patients, ECG, laboratory examination, symptoms or transthoracic echocardiography in rest could not rule out CAD or progress of known CAD. The hypothesis of the study is that detection of CAD can be improved by adding biomarkers to stress testing for the diagnostic workup of patients with suspected CAD or progress of already known CAD.


Recruitment information / eligibility

Status Completed
Enrollment 850
Est. completion date April 30, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Every patient referred to coronary angiography, or diagnostic work-up with suspicion of CAD or progress of CAD (in case of CABG patients or already treated with PCI) Exclusion Criteria: 1. Insufficient knowledge of the German language (able to understand and write the German language) 2. Physical or psychological incapability to take part in the investigation 3. Persons with no sufficient language ability in German to understand the provided study information material.

Study Design


Locations

Country Name City State
Germany Department of General and Interventional Cardiology, University Heart Center Hamburg Hamburg

Sponsors (1)

Lead Sponsor Collaborator
Universitätsklinikum Hamburg-Eppendorf

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnosis of coronary artery disease The diagnosis of coronary artery disease through stress testing alone and combined with cardiac biomarkers. Within the initial diagnostic evaluation process (maximum within 30 days)
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