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Clinical Trials/NCT05472207
NCT05472207
Recruiting
Not Applicable

"Multifactorial Risk Stratification in Acute and Chronic Cardiovascular Disease" ("riskINN ")

Medical University Innsbruck2 sites in 1 country5,000 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
Medical University Innsbruck
Enrollment
5000
Locations
2
Primary Endpoint
combination of cardiovascular mortality, stroke, myocardial infarction and hospitalization due to decompensated heart failure
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The aim of this study is to develop risk prediction models for the early detection of high-risk patients with structural, rhythmological or inflammatory cardiovascular diseases.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
January 2030
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Medical University Innsbruck
Responsible Party
Principal Investigator
Principal Investigator

Univ. Prof. Dr. Axel Bauer

Univ.-Prof. Dr.

Medical University Innsbruck

Eligibility Criteria

Inclusion Criteria

  • Decision-eligible male and female patients ≥18 years of age
  • Acute or chronic condition due to structural, rhythmologic, or inflammatory cardiovascular disease
  • Informed consent for participation in the clinical trial

Exclusion Criteria

  • missing infromed consent
  • pregnant or breast-feeding women

Outcomes

Primary Outcomes

combination of cardiovascular mortality, stroke, myocardial infarction and hospitalization due to decompensated heart failure

Time Frame: from inclusion to end of study (max. 4 years)

Secondary Outcomes

  • hospitalization due to decompensated heart failure(from inclusion to end of study (max. 4 years))
  • severe arrythmic events(from inclusion to end of study (max. 4 years))
  • cardiovascular mortality(from inclusion to end of study (max. 4 years))
  • hospitalization due to cardiovascular condition(from inclusion to end of study (max. 4 years))
  • admission to intensive care unit(from inclusion to end of study (max. 4 years))
  • myocardial infarction(from inclusion to end of study (max. 4 years))
  • total mortality(from inclusion to end of study (max. 4 years))
  • stroke(from inclusion to end of study (max. 4 years))

Study Sites (2)

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