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NCT06998355Withdrawn

BE.Amycon Registry UZ Leuven

BE.Amycon Amyloidosis Data Registry UZ Leuven

Source: ClinicalTrials.gov · Last updated 25 Sept 2026

Brief summary (registry, in English)

The goal of this observational study is to establish database with (limited) personal and health data of patients diagnosed with amyloidosis (any subtype) in order to get better insights on the disease presentation, disease evolution pattern, treatment plans and responses and survival.

Status (registry)
Withdrawn
Study type
Observational
Enrollment
0 (actual)
First submitted
12 May 2025
Start date
1 Sept 2025
Primary completion date
31 Dec 2027
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Diseases
Amyloidosis
NCT number
NCT06998355

Who cannot take part

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

Other

  • Not able to provide informed consent
  • Not willing to sign informed consent

Who the study is looking for

  • Age 18 years or older
  • Provide consent and sign informed consent form
  • Confirmed diagnosis of amyloidosis (any subtype), systemic and/or localised
  • Newly diagnosed or in follow-up during the study time-frame (1 JUN 2025 until 31 DEC 2027)

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
UZ Leuven Gasthuisberg
Coordinator of this site? Confirm its status
LeuvenBelgiumUnknown status

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