Institutional Registry of Haemorrhagic Hereditary Telangiectasia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorHospital Italiano de Buenos Aires
The purpose of this study is to create an institutional and population-based registry of Haemorrhagic Hereditary Telangiectasia with a prospective survey based on epidemiological data, risk factors, diagnosis, prognosis, treatment, monitoring and survival.
This study will also describe the occurrence of Haemorrhagic Hereditary Telangiectasia in the population of HIBA in the Central Hospital, as well as the characteristics of clinical presentation and evolution.
Patients with HHT defined.
Followed in Unidad HHT of Hospital Italiano de Buenos Aires.
None
Map coordinates are unavailable for these locations. Locations are shown below instead.