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Risk Stratification Using PET in HCM (HCM-PET)

R

Region Gävleborg

Status

Unknown

Conditions

Hypertrophic Cardiomyopathy

Treatments

Diagnostic Test: Positron Emission Tomography

Study type

Observational

Funder types

Other

Identifiers

NCT03278457
2017021

Details and patient eligibility

About

The overall rationale is to reduce the risk of sudden cardiac death in individuals with hypertrophic cardiomyopathy (HCM). The novel approach of this study is to correlate Positron Emission Tomography (PET) findings to ventricular arrhythmias detected by the implantable cardioverter defibrillator (ICD). This could potentially lead to an improved risk stratification of HCM patients.

Full description

Positron Emission Tomography (PET) is a functional imaging technique that utilizes radioactive tracers to gain information on physiological or pathophysiological processes in vivo. Different tracers can provide information on different processes of interest. In cardiology, metabolic processes consuming oxygen (aerobic) can be studied with 11-Carbon-Acetate, sympathetic innervation can be studied with 11-Carbon-hydroxyephedrine and using 15-Oxygen-water the myocardial blood flow. Structural information of the heart such as left ventricular mass, left ventricular volumes and wall thickness can also be calculated with PET.

The aim is to correlate PET parameters and burden of ventricular arrhythmias in order to improve risk stratification in HCM.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hypertrophic cardiomyopathy, implantable cardioverter defibrillator, informed consent

Exclusion criteria

  • Patients younger than 18 years, pregnancy, breast feeding, claustrophobia, intolerance/allergic reaction to adenosin or mannitol, severe hypotension, unstable angina pectoris, incompensated systolic heart failure, increased intracranial pressure, hypovolemia, dipyramidole.

Trial contacts and locations

1

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Central trial contact

Peter Magnusson, MD; Jonny Nordström, MSc

Data sourced from clinicaltrials.gov

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