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Taking people in GermanyNo phase

Studies tiny blood vessels in the eye in people with Fabry disease

Observes retinal blood vessels in adults with Fabry disease, looking for a noninvasive marker.

Plain-language title generated from the registry record
Registry title: Characterizing the Retinal Microvasculature in Patients with Fabry Disease: a Prospective Observational Study

Key facts

Where
München, GermanySee the site

Where in Germany

  • Department of nephrology, Klinikum rechts der IsarMünchen, GermanyTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Technical University of Munich
Trial code
NCT06758648
Record updated
6 January 2025
Original description
This study aims to gain a deeper understanding of endothelial dysfunction in patients with Fabry disease through a prospective study of the retinal microvasculature and to identify an objective, non-invasive marker to assess disease severity and cardiovascular risk in patients.Read full original descriptionShow less

Characterizing the Retinal Microvasculature in Patients with Fabry Disease: a Prospective Observational Study

This study aims to gain a deeper understanding of endothelial dysfunction in patients with Fabry disease through a prospective study of the retinal microvasculature and to identify an objective, non-invasive marker to assess disease severity and cardiovascular risk in patients.

The main questions addressed are: Do dynamic and static retinal vessel analysis parameters differ from those in healthy individuals? Can these parameters predict cardiovascular and/or Fabry-related events during follow-up? Do these parameters change during follow-up in patients with a non-stable disease?

Inclusion: Age > 18 years; Diagnosis of Fabry disease by genetic testing or GB3 activity in leukocytes; Signed informed consent form.

Exclusion: Surgery less than 2 weeks prior to inclusion in the study; Active infection or cancer; Known epilepsy; Known glaucoma; Lack of capacity to give consent; lack of informed consent.

ClinicalTrials.gov NCT06758648