Heart Failure / Cardiovascular Disease / Heart Disease · Observational Study
ClinicalTrials.gov · August 20, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a prospective observational study registered at ClinicalTrials.gov assessing whether standardised physician training on 2023 ESC heart failure guidelines improves real-world uptake of guideline-directed medical therapy (GDMT) for HFrEF in German hospitals. No outcome data are reported in this registry record; the study is currently active but not recruiting.
Observational. Heart Disease, Heart Failure, Cardiovascular Disease, Heart Failure, Systolic; age from 18 Years; to 130 Years. Intervention: Standardised physician training on 2023 ESC guideline-directed medical therapy (GDMT) for HFrEF, including rapid in-hospital initiation and up-titration of ARNI/ACE-I/ARB, beta-blockers, MRA, and SGLT2i.. n = 338. 6 sites: Germany.
This is a prospective observational study registered at ClinicalTrials.gov assessing whether standardised physician training on 2023 ESC heart failure guidelines improves real-world uptake of guideline-directed medical therapy (GDMT) for HFrEF in German hospitals. No outcome data are reported in this registry record; the study is currently active but not recruiting.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
This is an active observational registry study with no results posted; it describes a planned assessment of real-world GDMT implementation in German hospitals following physician training, but outcomes and effectiveness data are not yet reported.
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Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06675552). This is a study registration, not published results. Lead sponsor: AstraZeneca. Recruitment status: ACTIVE_NOT_RECRUITING. Study type: OBSERVATIONAL. Enrollment: 338 participants (ACTUAL). Conditions: Heart Disease, Heart Failure, Cardiovascular Disease, Heart Failure, Systolic. Primary outcome measures: Proportion of patients treated with HFrEF GDMT , Baseline to hospital discharge, on average 6 days after hospitalization/baseline. Brief summary: Heart failure (HF) is a global public health issue that affects more than 63 million people worldwide. The clinical and economic burden of HF on health care systems is substantial. Heart failure with reduced ejection fraction (HFrEF) represents approximately 50% of the HF patient population.The burden of HF is expected to increase substantially as the population ages, and despite improvements in treatment, hospitalisation and mortality rates remain especially high in HFrEF patients. The current guideline recommendation of directed medical therapy for HFrEF combines four drug classes with proven prognostic benefit: Angiotensin receptor-neprilysin inhibitor (ARNI)/angiotensin converting enzyme inhibitors (ACE I)/angiotensin receptor blockers (ARB), betablockers (BB), mineralocorticoid receptor antagonists (MRA), and sodium-glucose co-transporter 2 inhibitors (SGLT2i). The 2023 ESC (European Society of Cardiology) HF guideline update additionally recommends a rapid in-hospital sequencing approach of guideline-directed medical therapy (GDMT) with frequent physician visits during the first 6 weeks post discharge. Studies investigating the implementation of GDMT in a real-world setting have shown that a significant proportion of patients did not receive the recommended drug combination therapy. Delayed initiation of GDMT contributes to the low number of patients receiving guideline concordant HFrEF therapy, which ultimately may affect patient outcomes. One approach to implement the 2023 ESC guideline updates for heart failure treatment regarding early in-hospital initiation and rapid up-titration of GDMT could be to provide specific training on GDMT recommendations. Such a standardised training is offered to the physicians treating HF patients within selected hospitals of the German Helios hospital network (Helios-GDMT-program). Evidence is needed in order to assess whether in-hospital initiation and up-titration of all phenotype concordant classes of GDMT at hospital discharge can be observed after standardised physician training and whether the GDMT-program implementation also translates into real-world routine outpatient care with respect to use of GDMT and clinical outcomes.
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