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RECRUITINGINTERVENTIONAL

Effects of Low-Sodium Salt on Death, HF Hospitalization/ Emergency Department Visits and Quality of Life in HF Patients

Effects of Low-Sodium Substitute Salt on Death, Heart Failure Hospitalization, Heart Failure Emergency Department Visits, and Quality of Life in Patients With Heart Failure: A Multicenter, Double-Blind, Randomized Controlled Trial

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This study aims to investigate whether using a low-sodium substitute salt can help improve outcomes for patients with heart failure. Specifically, it will examine if the low-sodium substitute salt can reduce death rates, hospital readmissions, and emergency visits, as well as improve the quality of life for these patients.

Who May Be Eligible (Plain English)

Who May Qualify: 1. Aged between 18 and 75 years; 2. Hospitalized due to heart failure in the past year; 3. NYHA functional class II-III; 4. Echocardiographic evidence of LVEF \< 40% within the past 6 months; 5. Receiving guideline-directed medical therapy for heart failure; 6. Stable heart failure status, defined as heart failure stability for more than 4 weeks, with no increase in diuretic dose within the past 4 weeks; 7. Having a primary caregiver and frequently dining together at home; 8. Consuming commercially processed food no more than once a week; 9. Providing written willing to sign a consent form. Who Should NOT Join This Trial: 1. End-stage heart failure; 2. Hospitalization due to cardiovascular causes within the past month; 3. Uncorrected hyponatremia (Na \< 130 mmol/L); 4. Dialysis-dependent patients, or eGFR \< 20 mL/min/1.73m²; 5. Uncontrolled hyperglycemia, with fasting blood glucose \> 16 mmol/L; 6. Malignant cancer patients with a life expectancy of less than 1 year; 7. Conditions that, in the investigator's opinion, may interfere with adherence to the protocol, such as habitual reliance on takeout meals or dining at company cafeterias; 8. Planned hospitalization during the study period; 9. Unexplained weight loss greater than 5 kg in the past year; 10. The subject or family members have concerns about using the salt substitute in this study, or are planning for pregnancy, pregnant, or breastfeeding; 11. Another family member is already participating in this study; 12. The subject or family members are participating in other interventional clinical trials. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. Aged between 18 and 75 years; 2. Hospitalized due to heart failure in the past year; 3. NYHA functional class II-III; 4. Echocardiographic evidence of LVEF \< 40% within the past 6 months; 5. Receiving guideline-directed medical therapy for heart failure; 6. Stable heart failure status, defined as heart failure stability for more than 4 weeks, with no increase in diuretic dose within the past 4 weeks; 7. Having a primary caregiver and frequently dining together at home; 8. Consuming commercially processed food no more than once a week; 9. Providing written informed consent. Exclusion Criteria: 1. End-stage heart failure; 2. Hospitalization due to cardiovascular causes within the past month; 3. Uncorrected hyponatremia (Na \< 130 mmol/L); 4. Dialysis-dependent patients, or eGFR \< 20 mL/min/1.73m²; 5. Uncontrolled hyperglycemia, with fasting blood glucose \> 16 mmol/L; 6. Malignant cancer patients with a life expectancy of less than 1 year; 7. Conditions that, in the investigator's opinion, may interfere with adherence to the protocol, such as habitual reliance on takeout meals or dining at company cafeterias; 8. Planned hospitalization during the study period; 9. Unexplained weight loss greater than 5 kg in the past year; 10. The subject or family members have concerns about using the salt substitute in this study, or are planning for pregnancy, pregnant, or breastfeeding; 11. Another family member is already participating in this study; 12. The subject or family members are participating in other interventional clinical trials.

Treatments Being Tested

OTHER

low-sodium substitute salt

This study specifically customized sodium reducing substitute salts with a sodium chloride content not exceeding 62% and without the addition of potassium chloride.

Locations (1)

Anzhen Hospital, Capital Medical University
Beijing, Beijing Municipality, China