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NCT05101304Recruiting

Registre HEAR, Healthcare European Amyloidosis Registry

Source: ClinicalTrials.gov · Last updated 1 Nov 2021 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a non-interventional, prospective, retrospective, non-comparative, multi-center study. In order not to interfere with patient management, the study is observational. Thus, no follow-up visit is imposed. The data collection will be limited to the data related to the management of the patients included throughout their follow-up. This study is intended for all patients with a confirmed or suspected diagnosis of cardiac amyloidosis. Three cohorts will be identified: the HEAR (Healthcare European Amyloidosis Registry)-Retrospective Cohort, the HEAR(Healthcare European Amyloidosis Registry)-Retrospective-Prospective Cohort and the HEAR (Healthcare European Amyloidosis Registry)-Prospective Cohort.

Status (registry)
Recruiting
Study type
Observational
Enrollment
5000 (estimated)
First submitted
5 Oct 2021
Start date
29 Jun 2021
Primary completion date
30 Jun 2027
Lead sponsor
Saving Lives Matters
Diseases
Amyloidosis
NCT number
NCT05101304

What you commit to

  • Study type: Observational
  • Planned participants: 5000
  • From 29 Jun 2021 to the primary completion date, 30 Jun 2027
  • 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.

Who the study is looking for

  • Patients must meet all of the following inclusion criteria to be included in the study:
    • Major patient
    • Protected adult patient (guardianship or curatorship)
  • Prospective Cohort:
    • Patients referred or who have been referred to the participating centre for suspected amyloidosis.
    • Patient who signed the patient information "Prospective Cohort" note
  • Retro-prospective Cohort:
    • Patient already followed in the center with a confirmed diagnosis of amyloidosis Patient who signed the "retro-prospective cohort" patient information note
  • Retrospective cohort:
    • Deceased patients followed in the center with a confirmed diagnosis of amyloidosis
    • Study participants will not be compensated for their participation

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
Hopital Henri Mondor
Coordinator of this site? Confirm its status
CréteilFranceRecruiting

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