Imaging for the Evaluation of Transthyretin Cardiac Amyloidosis Prevalence of Patients Over 65 Hospitalized in Cardiology Wards (the IMPACT Study)

Sponsor
Poitiers University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05064839
Collaborator
Pfizer (Industry)
400
1
1
24
16.7

Study Details

Study Description

Brief Summary

Heart failure with preserved ejection and hypertrophic cardiomyopathy are common diseases and often associated with transthyretin cardiac amyloidosis (TTR-CM), especially in elderly people. Nevertheless, research of TTR-CM is recommended in patients with ventricular hypertrophy without other cause such as valvular disease or hypertension. Therefore, the exact prevalence of TTR-CM remains unknown. We aim to determine the prevalence of TTR-CM in patients with ventricular hypertrophy and aged ≥ 60 years old, hospitalized in our cardiology department (CHU de Poitiers) by performing bone scintigraphy and research of AL amyloidosis.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Bony scintigraphy
Phase 3

Detailed Description

Not Provided

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Imaging for the Evaluation of Transthyretin Cardiac Amyloidosis Prevalence of Patients Over 65 Hospitalized in Cardiology Wards (the IMPACT Study)
Actual Study Start Date :
Oct 6, 2021
Anticipated Primary Completion Date :
Oct 6, 2023
Anticipated Study Completion Date :
Oct 6, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Bony scintigraphy

Bony scintigraphy within 1 to 4 months after inclusion

Procedure: Bony scintigraphy
Bony scintigraphy (99mTc-Hydromethylene diphosphonate) will be performed in all patients with hypertrophy of the left ventricle

Outcome Measures

Primary Outcome Measures

  1. Percentage of patients with a positive bone scintigraphy (perugini score> or = 2) in the absence of AL cardiac amyloidosis. [At Visit 2, one to four months after inclusion visit.]

    Percentage of patients with a positive bone scintigraphy (perugini score> or = 2) in the absence of AL cardiac amyloidosis in patients over 60 years hospitalised in cardiology wards, with an hypertrophy of the left ventricle on transthoracic echocardiography (thickness of the left ventricle at the end of diastole >12mm), whatever the possible cause of hypertrophy of the left ventricle (other potential cause not excluded), and without prior diagnosis of cardiac amylosis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient ≥ 60 years, hospitalised in cardiology wards of the Centre Hospitalier Universitaire of Poitiers

  • Left ventricle hypertrophy on echocardiography

  • Patient able to comply with study procedures

  • Patient legally free and not subject to any custody, guardianship, tutelage or subordination measures

  • Patient having signed an informed consent after clear and fair information on the study

Exclusion Criteria:
  • CardiacTransplant

  • Complex congenital cardiopathies

  • Know diagnosis of amylosis

  • Contra-indication to bony scintigraphy : hypersensitivity to sodium oxidronate or one of its excipients, or to one of the components of radiopharmaceutic marked product ;

  • Subject not able to comply with study procedures

  • Patients not benefiting from a Social Security scheme or not benefiting from it through a third party

  • Persons benefiting from enhanced protection, namely minors, persons deprived of their liberty by a judicial or administrative decision, patients staying in a health or social establishment, adults under legal protection, and patients in emergency situation.

  • Women not menopausal

Contacts and Locations

Locations

Site City State Country Postal Code
1 C.H.U. de Poitiers Poitiers France 86000

Sponsors and Collaborators

  • Poitiers University Hospital
  • Pfizer

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Poitiers University Hospital
ClinicalTrials.gov Identifier:
NCT05064839
Other Study ID Numbers:
  • 2021-A00732-39
First Posted:
Oct 1, 2021
Last Update Posted:
Oct 11, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Poitiers University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 11, 2021