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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03966729
Other study ID # REDEAL-HF
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2009
Est. completion date December 31, 2023

Study information

Verified date July 2022
Source Wuerzburg University Hospital
Contact Peter Nordbeck, MD, PhD
Phone +49 931 201 39181
Email nordbeck_p@ukw.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study characterizes heart failure patients who attended the University Hospital Würzburg. The primary aim is a better understanding of the relationships and differences between the subgroups HFrEF (EF < 40%), HFmrEF (EF 40-49%), and HFpEF (EF>50%), contributing to an improved diagnosis, prognosis and therapy of patients with heart failure.


Description:

The varying clinical picture of heart failure (HF) represents a major challenge for patient care in Germany. HF is one of the most common reasons for hospitalization in the Western world. In the chronic course of heart failure, affected patients are committed to morbidity, lifelong therapy and high risk of cardiac decompensation, also associated with high mortality. Heart failure patients, who visited the Cardiology Department of the University Hospital Wuerzburg, shall be analyzed with regard to all clinical data and outcome. This retrospective work should help to better understand the three groups HFrEF (EF < 40%), HFmrEF (EF 40-49%) and HFpEF (EF>50%) and help identifying similarities and differences between the groups. Hereby we hope for progress in diagnostic, prognostic and therapeutic aspects of heart failure.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis: Heart failure - Minimum of two echocardiographic examinations in a minimum time frame of six months - Patients must have reached the age of 18

Study Design


Intervention

Other:
Time (outcome)


Locations

Country Name City State
Germany University Hospital Würzburg Würzburg Bavaria

Sponsors (1)

Lead Sponsor Collaborator
Wuerzburg University Hospital

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Long-term survival in heart failure patients with preserved, mid-range or reduced left ventricular ejection fraction Survival of patients with heart failure extracted from medical record or by telephone interview 1 year follow up after last examination
Secondary Impact of clinical imaging and laboratory parameters on long-term survival in heart failure patients with precerved, mid-range or reduced left ventricular ejection fraction Parameters are derived from standard echocardiography, cardiac magnetic resonance imaging and blood testing. 6 months
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