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This study investigates the effects of ultrafiltration treatment in heart failure patients, aiming to evaluate primary endpoints such as weight loss and dyspnea score at 48 hours. Secondary endpoints include net fluid loss, worsening heart failure within 90 days, and freedom from rehospitalization. The study outlines methods for inclusion and exclusion criteria, procedures, statistical analyses, and safety endpoints such as serum creatinine changes and adverse events. The findings will contribute to understanding the efficacy and safety of ultrafiltration in managing heart failure.
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