Status: Recruiting
Institutional Registry of Haemorrhagic Hereditary Telangiectasia
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.
Participants needed: 590
Trial details
Biological sex: AllType: ObservationalSponsor: Hospital Italiano de Buenos AiresUpdated: May 22, 2025Locations: 1
Eligibility criteria
Patients with HHT defined. [+1]