Last updated on December 2018

Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF

Brief description of study

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 Study Identifier: NCT03547583

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Bayer Clinical Trials Contact

Institute Jantung Negara
Kuala Lumpur, Malaysia
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Recruitment Status: Open

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