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NCT04327479 Clinical Trial

Characterization of Cardiovascular Diseases and Risk Factors in Patients With Suspected SARS-CoV2/Covid-19 Infection

Cardiovascular Diseases Clinical Trial

Official title:
Characterization of Cardiovascular Diseases and Risk Factors in Patients With Suspected SARS-CoV2/Covid-19 Infection

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04327479
Other study ID # 20-9213-BO
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 26, 2020
Est. completion date July 25, 2022

Study information
Verified date November 2022
Source University Hospital, Essen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infects host-cells via ACE2-receptors, which leads to pneumonia (COVID-19) but also can lead to myocarditis (acute myocardial injury) and chronic damage to the cardiovascular system. Therefore, cardiovascular protection may be necessary when treating patients with COVID-19 infection. This may especially be necessary in patients with cardiovascular diseases, risk factors, and co-medication.

Recruitment information / eligibility
Status Completed
Enrollment 728
Est. completion date July 25, 2022
Est. primary completion date March 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with suspected SARS-CoV2/Covid-19 infection Exclusion Criteria: - Unwillingness to participate

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Assessment of cardiovascular diseases and cardiovascular risk factors
At inclusion, patients will be screened for pre-existing cardiovascular diseases and cardiovascular risk factors, as well as medication.

Locations
Country Name City State
Germany University Hospital Essen Essen NRW

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Essen

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary All-cause mortality mortality of any cause During 1 year follow-up
Secondary 30-day mortality mortality of any cause Within 30 days after inclusion
Secondary Major adverse cardiovascular events Myocardial infarction, stroke, or CV death During 1 year follow-up
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