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NCT07577466Not yet recruiting

Screening, Characterization, and Longitudinal Follow-up of Patients With Cardiac Amyloidosis

Source: ClinicalTrials.gov · Last updated 11 May 2026

Brief summary (registry, in English)

Cardiac amyloidosis is a progressive disorder caused by extracellular deposition of amyloid fibrils in the heart, leading to heart failure and impaired cardiac function. Early diagnosis and targeted therapies are essential to improve patient outcomes. This prospective, single-center study aims to longitudinally follow patients with suspected cardiac amyloidosis to characterize disease progression and assess treatment effects. Participants will undergo cardiac magnetic resonance imaging (resting and exercise stress MRI), magnetic resonance spectroscopy, cardiopulmonary exercise testing (spiroergometry) and blood testing at baseline and at 6, 12, and 24 months

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
4 May 2026
Start date
15 Jun 2026
Primary completion date
31 Dec 2029
Lead sponsor
Heinrich-Heine University, Duesseldorf
NCT number
NCT07577466

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 15 Jun 2026 to the primary completion date, 31 Dec 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Contraindications to cardiac MRI (e.g., metallic foreign bodies, older-generation pacemakers, severe obesity, claustrophobia)

Age

  • Age \< 18 years

Other

  • Lack of written informed consent for study participation
  • Inability to comply with the study procedures

Who the study is looking for

  • Age \> 18 years
  • Male and female patients undergoing clinically indicated diagnostic work-up for amyloidosis or with a previously confirmed diagnosis of cardiac amyloidosis prior to initiation of therapy
  • Presence of left ventricular wall thickness \> 12 mm on transthoracic echocardiography and at least one "red flag" suggestive of cardiac amyloidosis (according to ESC 2021 criteria) or an otherwise clinically established suspicion of amyloidosis
  • Written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Duesseldorf
Coordinator of this site? Confirm its status
DüsseldorfGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.