RecruitingNCT01761981
Institutional Registry of Haemorrhagic Hereditary Telangiectasia
Sponsor
Hospital Italiano de Buenos Aires
Enrollment
590 participants
Start Date
Jan 1, 2010
Study Type
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria2
- Patients with HHT defined.
- Followed in Unidad HHT of Hospital Italiano de Buenos Aires.
Exclusion Criteria1
- \. Denied to participated in the registry or inform consent process.
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT01761981