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

Contact Investigators or Research Sites near you

Start Over

Bayer Clinical Trials Contact

Institute Jantung Negara
Kuala Lumpur, Malaysia
0.68miles
  Connect »

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


Receive Emails About New Clinical Trials!

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.