Aortic Stenosis and Cardiac Amyloidosis

NCT06129331 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2023-11-13

No results posted yet for this study

Summary

The dual pathology of aortic stenosis (AS) and cardiac amyloidosis (CA) is increasingly recognized. Even tough efforts have been undertaken to bring cohorts together, the largest cohort of AS-ATTR to date is \<50 patients. It is the aim of the present international, multi-center registry to collect \~300 patients with AS-CA creating a big enough cohort to allow

1. thorough characterization of this condition
2. assessment of log-term clinical outcomes of AS-CA
3. assessment of effectiveness of amyloid-specific treatment on top of valve replacement

Conditions

  • Cardiac Amyloidosis
  • Aortic Stenosis

Interventions

DRUG

Amyloid-specific treatment

Amyloid-specific treatment

OTHER

No amyloid-specific treatment

No amyloid-specific treatment

Sponsors & Collaborators

  • Allina Health System

    collaborator OTHER
  • Royal Free Hospital NHS Foundation Trust

    collaborator OTHER
  • Columbia University

    collaborator OTHER
  • Medical University of South Carolina

    collaborator OTHER
  • Laval University

    collaborator OTHER
  • Vilnius University Hospital Santaros Klinikos

    collaborator OTHER
  • Université Catholique de Louvain

    collaborator OTHER
  • Wolfson Medical Center

    collaborator OTHER_GOV
  • IRCCS Azienda Ospedaliero-Universitaria di Bologna

    collaborator OTHER
  • University of Trieste

    collaborator OTHER
  • Medical University of Vienna

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Austria
  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06129331 on ClinicalTrials.gov