Actively Recruiting

Age: 18Years +
All Genders
ID07154394

Investigation of Cardiac Amyloid Deposits as a Cause of Cardiac Dysfunction in Alzheimer's Disease

Led by University Hospital, Essen · Updated on 2025-09-04

15

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the possible shared causes of cardiac amyloidosis and Alzheimer's disease, both involving amyloid deposits. This observational study uses Positron Emission Tomography (PET) scans with amyloid tracers, typically used for Alzheimer's imaging, to also examine amyloid deposits in the heart. The goal is to improve diagnosis methods for both conditions by exploring their connection. Participants are patients clinically referred for cerebral amyloid PET scans to clarify an Alzheimer's diagnosis. In addition to the brain PET scan, the study adds cardiac PET/MRI imaging without extra substances or radiation. Participants also receive a transthoracic echocardiogram with strain analysis and a 12-lead electrocardiogram (EKG) as part of a comprehensive diagnostic assessment. During the study, each participant undergoes clinical dementia evaluation along with the imaging tests. Researchers observe the frequency of cardiac amyloid deposits overall and in relation to disease stages over about one year. The study includes regular heart and brain assessments to monitor amyloid presence and heart function, aiming to better understand their link in Alzheimer’s disease.

CONDITIONS

Brief Title

Cardiac Amyloid Deposits and Heart Dysfunction in Alzheimer's Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing cerebral amyloid PET examination for clinical indication to clarify Alzheimer's disease
  • No contraindications to undergo an MRI examination
  • No contraindications to undergo an Amyloid PET scan
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Patients with vascular dementia and confirmed other causes of dementia such as stroke, vitamin deficiency, thyroid insufficiency, or toxic causes like alcohol
  • Patients with pronounced cardiac preconditions
  • Pregnant and breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 1 day

Participants undergo a comprehensive diagnostic evaluation including cerebral amyloid PET, cardiac PET/MRI imaging, transthoracic echocardiogram with strain analysis, and a 12-lead electrocardiogram (EKG).

1 visit (in-person)

Long-term Monitoring

Duration - Approximately 1 year

Participants are observed over an average of 1 year to evaluate the frequency of cardiac amyloid deposits and their relation to Alzheimer's disease manifestations.

Trial Site Locations

Total: 1 location

1

University Hospital Essen

Essen, North Rhine-Westphalia, Germany, 45147

Actively Recruiting

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Research Team

D

David Kersting, MD PhD

S

Stephan Settelmeier, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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