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Active, Not Recruiting

NCT Number: NCT04064450

MyoVasc Study on the Development and Progression of Heart Failure

The MyoVasc - Study is an observational, prospective cohort study. The study is investigating the development and progression of the heart failure syndrome, phenotypes of the heterogeneous syndrome, and the interactions of phenotypes with the vasculature regarding their impact for the course of heart failure.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

35 year–84 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Medical Center of the Johannes Gutenberg-University Mainz

Mainz, Rhineland-Palatinate, 55131, Germany

About this study

"MyoVasc" is an observational cohort study investigating the development and progression of heart failure (HF). The primary objective of the study is: i, to advance the understanding of pathomechanisms of the heterogenous syndrome in the full range of clinical presentation, ii, to evaluate current clinical phenotypes of HF, and iii, to identify and describe homogenous subgroups with regard to disease development using a systems-oriented approach. A special focus is put on the investigation of heart failure with preserved ejection fraction in contrast to the more investigated and established phenotype with reduced ejection fraction. Further aspects comprise inter alia the relevance of metabolic dysregulation, inflammation and coagulation for the course of the disease.

The primary endpoint of the study is the combined outcome "worsening of heart failure" defined as transition from asymptomatic to symptomatic heart failure, hospitalization due to heart failure, or cardiac death. Secondary endpoints are the components of the primary endpoint, myocardial infarction, stroke, hospitalization due to cardiovascular disease, venous thromboembolism, atrial fibrillation, and all-cause death. Disease progression is monitored by a large panel of biomarkers for structure and function of cardiac and vascular systems and related organs.

Individuals aged 35- to 84-years with echocardiographic signs of heart failure irrespective of the clinical status are enrolled and a subsample of controls without heart failure. Individuals were recruited from health institutions and a population sample from the registration office. The study sample comprises approx. 3,200 individuals, of which N~2,700 individuals have heart failure and N~500 individuals are controls. Study participants receive a highly standardized 5-hour baseline examination in the study center with examinations of the cardiovascular system (e.g. anthropometrics, 2D- and 3D-echocardiography, carotid sonography, vascular function, ankle-brachial index, body plethysmography, capacity exercise testing, blood pressure measurements (resting, ABPM), ECG (12-lead, holter), computer-assisted personal interview, and venous blood withdrawal for bio banking). Annual follow-up examinations are performed via computer-assisted telephone interviews tracking comprehensively the participants´ health status, assessing current medication and recording clinical events. Every two years, the participant is invited again to the MyoVasc Study Center for the conduct of sequential follow-up investigations, which are identical to the initial examination.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Asymptomatic heart failure or symptomatic heart failure
  • Written consent
  • Sufficient knowledge of the German language, in order to understand study documents and computer assisted interview without any translation

Exclusion criteria

  • Individuals who are not able to visit the study center due to psychological or physical impairment
  • STEMI within the last 4 months, NSTEMI within the last 3 months
  • Acute decompensated heart failure
  • Surgery, especially coronary artery bypass grafting within the last 3 months
  • Acute disease, especially acute infectious disease, endocarditis, myocarditis or pericarditis

Treatment and study plan

Primary outcomes

  1. Incidence of Worsening of Heart Failure

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    The primary outcome "worsening of heart failure" differs between groups:

    • Population Controls: i.e. composite of cardiac death and incident heart failure (i.e. incident asymptomatic or symptomatic heart failure)
    • Individuals with asymptomatic heart failure: i.e. composite of cardiac death and transition from asymptomatic to symptomatic heart failure
    • Individuals with symptomatic heart failure: i.e. composite of cardiac death and hospitalization due to worsening of heart failure

Secondary outcomes

  1. Incidence of Cardiac death

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Cardiac death

  2. Incidence of Hospitalization due to heart failure

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Hospitalization due to heart failure

  3. Incidence of transition from asymptomatic to symptomatic heart failure

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Transition from asymptomatic to symptomatic heart failure

  4. Incidence of heart failure (i.e. incident asymptomatic or symptomatic heart failure) in controls

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Incident heart failure (i.e. incident asymptomatic or symptomatic heart failure) in controls

  5. Incidence of death

    Time frame: Follow-up of vital status for 10 years

    Death

  6. Incidence of hospitalization

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Hospitalization

  7. Incidence of myocardial infarction

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Myocardial infarction

  8. Incidence of stroke or transient ischemic attack

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Stroke or transient ischemic attack

  9. Incidence of cardiac arrhythmia

    Time frame: Continuous assessment throughout the follow-up of the study

    Cardiac arrhythmia

  10. Incidence of atrial fibrillation

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Atrial fibrillation

  11. Incidence of angina pectoris

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Angina pectoris

  12. Incidence of deep vein thrombosis

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Deep vein thrombosis

  13. Incidence of pulmonary embolism

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Pulmonary embolism

  14. Incidence of arterial hypertension

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Arterial hypertension

  15. Incidence of peripheral artery disease

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Peripheral artery disease

  16. Worsening of exercise capacity as assessed via peak oxygen uptake

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Assessment of peak oxygen uptake via cardiopulmonary exercise testing under consideration of the circulatory (blood pressure, heart rate, electrocardiogram) and respiratory response (ventilatory anaerobic threshold and reserve) by a trained physician

  17. Worsening of systolic cardiac function assessed by ventricular ejection fraction

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Assessed via 2D/3D transthoracic cardiac echocardiography by a trained physician

  18. Incidence of revascularization

    Time frame: Assessment in annual follow-up contacts over a period of 10 years

    Revascularization

  19. Worsening of diastolic cardiac function assessed by mitral inflow signal and tissue doppler of the heart

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6 and 8 years

    Assessed via 2D/3D transthoracic cardiac echocardiography by a trained physician

  20. Worsening of cardiac strain assessed by speckle-tracking of the heart

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Assessed via 2D/3D transthoracic cardiac echocardiography by a trained physician

  21. Worsening of renal function as assessed by glomerular filtration rate

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Worsening of renal function as assessed by estimated glomerular Filtration rate (eGFR) as humoral biomarker of renal function

  22. Worsening of pulmonary function as assessed by FEV1

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Worsening of forced expiratory volume in one second (FEV1) via body plethysmography

  23. Worsening of vascular function as assessed by FMD/FMC

    Time frame: Assessment in biannual follow-up contacts in a dedicated study center after 2, 4, 6, 8 and 10 years

    Worsening of flow-mediated dilatation (FMD) and constriction (FMC) of the radial artery

Sponsors and collaborators

Lead sponsor

Johannes Gutenberg University Mainz

Other

Registry information

Official study title

MyoVasc - An Epidemiological Cohort Study to Investigate the Development and Progression of Heart Failure and the Interaction With Vascular Disease

Important dates

Study start
2013
Primary completion
2028
Study completion
2028
First posted
Aug 22, 2019
Registry last updated
Aug 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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