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Clinical Trial Summary

Sacubitril/valsartan reduces the risk of cardiovascular mortality among patients with heart failure with reduced ejection fraction, and has been recently indicated as a new treatment option with a strong level of recommendation (class I, level of evidence B) in the main international guidelines. Cardiovascular disease (CVD) is the most common cause of death in end stage renal disease (ESRD) patients undergoing hemodialysis (HD). Hence, treatments to improve mortality and specifically cardiovascular outcomes in this population are greatly needed. So far, no data available about the efficacy and safety of sacubitril/valsartan in ESRD patients undergoing hemodialysis, although this medication was noted to be effective and comparably well tolerable in those with estimated glomerular filtration rate(eGFR) 20 to 60 mL/min/1.73 m2 in the United Kingdom Heart and Renal Protection-III trial.

The purpose of this open label, randomized controlled study with prospective data collection is to assess the efficacy and safety of sacubitril/valsartan in maintenance hemodialysis patients with heart failure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04458285
Study type Interventional
Source Guangdong Provincial People's Hospital
Contact Faye Jiang, Doctor
Phone (+86)020-83525210
Email gdphgcp@gdph.org.cn
Status Recruiting
Phase N/A
Start date January 1, 2020
Completion date December 31, 2020

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