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Clinical Trials in Denmark / NCT07493590
Starting soon Observational

CAPTURE-HFpEF: National Study of Identification and Phenotyping of Heart Failure With Preserved Ejection Fraction

NCT07493590 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2026-04-01
Last updated
2026-03-25

Condition(s) studied

Heart Failure With Preserved Ejection Fraction (HFPEF)

Investigational drug(s) / intervention(s)

HFpEF Observational Measurements

HFpEF Observational Measurements: Observational measurements including collection of blood for biomarker and genetic analyses, echocardiography, ECG, and extraction of clinical data from electronic health records (comorbidities, medications, and prior hospitalizations). No treatment or procedure is assigned; all data reflect routine care and participant characteristics.

Study summary

The goal of this observational study is to improve early detection, characterization, and understanding of heart failure with preserved ejection fraction (HFpEF) in adults at risk of or diagnosed with HFpEF, including men and women across Danish regions.

The main questions to answer are:

Can systematic cardiovascular screening and deep phenotyping improve early identification and classification of HFpEF?

Which clinical, imaging, biomarker, and metabolic characteristics define subtypes (phenotypes) of HFpEF and predict disease progression and outcomes?

Researchers will compare participants with HFpEF, participants at risk of HFpEF, and relevant control groups to see if differences in biomarkers, imaging findings, and clinical characteristics can identify early disease stages and distinct HFpEF phenotypes.

Participants identified with HFpEF will:

* Undergo detailed cardiovascular examinations (e.g., echocardiography, CT and other imaging examinations, RHC, CPET)
* Provide blood and tissue samples for biomarker and metabolic analyses
* Complete clinical assessments and questionnaires
* Have relevant health data collected from national health registries
* Attend follow-up assessments to monitor disease progression

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Patients \>60 years with ≥1 risk factor, OR * Patients \>50 years with ≥2 risk factors * Hypertension * Type 1 or 2 diabetes * Chronic kidney disease (eGFR \<60 mL/min/1.73 m²) * Previous cardiotoxic drug exposure * atrial fibrillation * Ischemic heart disease * Previous heart valve surgery/intervention * Body mass index \>30 kg/m² (self-reported) * Use of ≥40 mg furosemide * Obstructive sleep apnea * Non-alcoholic fatty liver disease Exclusion Criteria: * Cancer \<1 year * Dialysis * COPD and O2 * Nursing home * Age \>90 years * Dementia * Known dilated cardiomyopathy * Prior organ-transplantation * Amyloidosis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Herlev and Gentofte Hospital Copenhagen Denmark

More Herlev and Gentofte Hospital trials in Denmark

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07493590 on ClinicalTrials.gov ↗ ← All trials in Denmark