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Heart Failure-USB: Prediction and Progression

Heart Failure-USB: Prediction and Progression

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04000061
Enrollment
6000
Registered
2019-06-27
Start date
2019-06-13
Completion date
2026-12-31
Last updated
2025-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Acute Heart Failure, Heart Failure

Brief summary

This retrospective cohort study is to identify triggers of heart failure (HF) development and drivers of HF progression as well as the underlying cardiac disease (phenotype) to identify patients at risk and predict the clinical course of the disease. Data of patients who were hospitalized during the years 2010-2023 with acute coronary syndrome (ACS) and/ or with acute heart failure (AHF) will be collected and analyzed. In a subgroup cohort efficacy and safety of digoxin in patients with acute heart failure triggered by tachyarrhythmia will be evaluated.

Interventions

OTHERmedical chart review

data generated by medical review include Medical history, Medications at presentation, during hospitalization and at discharge, New York Heart Association (NYHA) class, Killip class, Electrocardiographic (ECG) data, echocardiographic data, Interventions (Percutaneous Coronary Intervention (PCI), Coronary Artery Bypass Graft (CABG), Implantable Cardioverter Defibrillator (ICD) implantation, Cardiac Resynchronization Therapy (CRT) Implantation), Outcome Information: all-cause death, HF hospitalizations

OTHERdata generated by direct IT export

data generated by direct IT export include Anthropometric data (age, sex, height, weight), Vital signs, Laboratory data

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients hospitalized with a primary diagnosis of ACS * Patients hospitalized with a primary or secondary diagnosis of AHF

Exclusion criteria

* Existence of a documented statement of the patient against the scientific use of clinical data

Design outcomes

Primary

MeasureTime frameDescription
number of all-cause death1 to 8 years after hospitalizationnumber of all-cause death in patients hospitalized with ACS and AHF during the years 2010-2023.
number of HF hospitalizations1 to 8 years after hospitalizationnumber of new HF hospitalizations in patients hospitalized with ACS and AHF during the years 2010-2023
number of cardiovascular death1 to 8 years after hospitalizationnumber of cardiovascular death in patients hospitalized with ACS and AHF
number of cardiovascular hospitalizations1 to 8 years after hospitalizationnumber of cardiovascular hospitalizations

Countries

Switzerland

Contacts

Primary ContactChristian Müller, Prof. Dr.
Christian.mueller@usb.ch0041 6132 86 549
Backup ContactFiona Nafaa, MD
fiona.nafaa@usb.ch+41 61 32 87747

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026