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Metabolic Abnormalities, Lifestyle and Diet Pattern in Heart Failure (MALD-HF)

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Enrolling

Conditions

Metabolic Disease
Heart Failure

Study type

Observational

Funder types

Other

Identifiers

NCT03951311
RJ-20172004

Details and patient eligibility

About

Metabolic abnormalities (e.g., hypertension, diabetes mellitus, dyslipidemia, and obesity) and unhealthy lifestyle behaviors (e.g., smoking and drinking habits, sedentary behavior, sleep disorder and physical inactivity) and unhealthy diet (e.g., high sugar and high fat) are major risk factors for cardiovascular diseases mobility and mortality. The investigators sought to estimate the impact of metabolic abnormalities, lifestyle behavior and diet pattern on prognosis of heart failure. This study planned to consecutively enroll 1,500 participants with heart failure with reduced ejection fraction and heart failure with mid-range ejection fraction fulfilling the inclusion criteria. Each heart failure survivors will be followed up for 5 years. Information on metabolic diseases, lifestyle and diet pattern were obtained through standardized questionnaire. The major adverse cardiac events will be identified by reviewing pertinent medical records and discharge lists from the hospitals, or official death certificates collected at local death registration centers, or directly contacting participants' family. The Cox proportional hazard model will be used to assess the association between metabolic risk factors and lifestyle and diet habits and health outcomes in heart failure patients.

Enrollment

1,500 estimated patients

Sex

All

Ages

14 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. aged 14 years or older;
  2. typical symptoms of heart failure according to the Framingham criteria;
  3. left ventricular ejection fraction (LVEF) <50%, demonstrated by echocardiography or cardiac magnetic resonance, which include either patients with mid-range EF (HFmEF) or with reduced EF (HFrEF) with relevant structural and functional cardiac changes and/or elevated N-terminal pro-brain B-type natriuretic peptide (pro-BNP) (e.g., ≥400 pg/mL).

Exclusion criteria

  1. age <14 years or ≥90 years;
  2. pregnancy;
  3. cancer with a life expectancy of less than one year;
  4. participation in other trials;
  5. endocarditis, pericardial diseases, or congenital heart diseases;
  6. heart failure secondary to non-cardiac diseases (e.g., pulmonary heart disease, infection, infiltration, metabolic derangements, severe anemia, sepsis, and arteriovenous fistula);
  7. lack of informed consent;
  8. refusal of the drug treatment or intervention recommended by the guidelines.

Trial contacts and locations

1

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Central trial contact

Zhijun Wu, MD

Data sourced from clinicaltrials.gov

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