Phase
Condition
Congestive Heart Failure
Chest Pain
Heart Disease
Treatment
N/AClinical Study ID
Ages 18-130 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age ≥18 years at the time of signing the informed consent
Hospitalised in a participating site and receiving full inpatient treatment (atleast 24h hospital stay)
Diagnosis of HFrEF according to the current guidelines of the European Society ofCardiology (ESC) with a left ventricular EF of ≤40% (as measured perechocardiography during the index hospital stay or within 3 months prior to indexhospitalisation with available reports from imaging (ejection fraction) at the timeof study inclusion)
Treated with a maximum of 2 of the indicated drug classes (ACE-I/ARNI/ARB, BB, MRA,SGLT2i) according to guideline recommendation (GDMT) at admission.
Signed and dated written informed consent prior to enrolment in the study
Willing and capable to fulfil requirements listed in the ICF
Exclusion
Exclusion Criteria:
Initial presentation (index hospitalisation) in cardiogenic shock or other kinds ofshock
Status post heart transplantation
History of intolerance to one or more GDMT drug classes (ACE-I/ARNI/ARB, BB, MRA,SGLT2i) or significant side effects that led to the discontinuation of two or moresubstances within one drug class (except from ACE-I/ARB, e.g., if 2 different ACEinhibitors triggered cough, but sartans are tolerated, then the patient is notexcluded)
Current or planned participation in a clinical trial
Decision by the investigator that the participant should not participate in thestudy if the participant is unlikely to comply with study procedures
Pregnancy or breast-feeding
Study Design
Study Description
Connect with a study center
Research Site
Erfurt, 99089
GermanyActive - Recruiting
Research Site
Gifhorn, 38518
GermanyActive - Recruiting
Research Site
Leipzig, 04289
GermanyActive - Recruiting
Research Site
Schwerin, 19049
GermanyActive - Recruiting
Research Site
Wuppertal, 42117
GermanyActive - Recruiting
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