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Clinical Trial Summary

The primary hypothesis in this trial is that the treatment with vericiguat 10 mg or 15 mg in patients with HFpEF improves the KCCQ PLS (Kansas City Cardiomyopathy Questionnaire Physical limitation score) compared to placebo after 24 weeks of treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Chronic Heart Failure With Preserved Ejection Fraction
  • Heart Failure

NCT number NCT03547583
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date June 15, 2018
Completion date November 4, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT04944706 - Efficacy and Safety of Qishenyiqi Dripping Pills for Treating Chronic Heart Failure With Preserved Ejection Fraction Phase 2