Recruiting NCT05472207
"Multifactorial Risk Stratification in Acute and Chronic Cardiovascular Disease"
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Cardiovascular Diseases, Healthy. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Austria
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
"Multifactorial Risk Stratification in Acute and Chronic Cardiovascular Disease" ("riskINN ")
Overview
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.
Primary outcome measures
- 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 outcome measures (8)
- total mortality [Time frame: from inclusion to end of study (max. 4 years)]
- cardiovascular mortality [Time frame: from inclusion to end of study (max. 4 years)]
- stroke [Time frame: from inclusion to end of study (max. 4 years)]
- myocardial infarction [Time frame: from inclusion to end of study (max. 4 years)]
- hospitalization due to decompensated heart failure [Time frame: from inclusion to end of study (max. 4 years)]
- hospitalization due to cardiovascular condition [Time frame: from inclusion to end of study (max. 4 years)]
- admission to intensive care unit [Time frame: from inclusion to end of study (max. 4 years)]
- severe arrythmic events [Time frame: from inclusion to end of study (max. 4 years)]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Austria · 2 centers
- Medizinische Universität Innsbruck, Universitätsklinik für Innere Medizin III, Kardiologie — Innsbruck
- Reha Zentrum Münster — Münster
Identifiers
NCT: NCT05472207 · 1328/2020