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Clinical Trials/NCT01761981
NCT01761981
Recruiting
Not Applicable

Institutional Registry of Haemorrhagic Hereditary Telangiectasia

Hospital Italiano de Buenos Aires1 site in 1 country590 target enrollmentJanuary 1, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Haemorrhagic Hereditary Telangiectasia
Sponsor
Hospital Italiano de Buenos Aires
Enrollment
590
Locations
1
Primary Endpoint
morbidity
Status
Recruiting
Last Updated
11 months ago

Overview

Brief 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.

Detailed Description

Haemorrhagic Hereditary Telangiectasia is a uncommon autosomic hereditary disorder caracterizad for recurrent epistaxis,cutaneomucous telangiectasias and arteriovenous malformations in diferent organs; brain, lung, liver and gastrointestinal are more often afected . Afect one in 5000-8000 individual in worldwide. HHT may produce important morbidity like brain absces, stroke, hemoptisis and cronic ferropenic anemia. Molecular mechanism of this disorder are complex and still no fully dilucidated. The genes mutated in HHT encode endothelial cell-expressed proteins that mediate signalling by the transforming growth factor (TGF)b superfamily. Endoglin (HHT type I) and ACVRL-1 (HHT type 2) mutations are responsible in more than 80% of the individuals. Mutation of SMAD 4 protein (MADH4)cause HHT in association with juvenile polyposis. HHT may associated with primary pulmonary hypertension en more rare cases. There are not HHT registry in Argentina and Latinamerican population. This registry may gader valious information in order to generate a better diagnosis and treatment of our population and others.

Registry
clinicaltrials.gov
Start Date
January 1, 2010
End Date
December 2035
Last Updated
11 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

MARCELO MARTIN SERRA

Marcelo Martin Serra

Hospital Italiano de Buenos Aires

Eligibility Criteria

Inclusion Criteria

  • Patients with HHT defined.
  • Followed in Unidad HHT of Hospital Italiano de Buenos Aires.

Exclusion Criteria

  • Denied to participated in the registry or inform consent process.

Outcomes

Primary Outcomes

morbidity

Time Frame: 1 year

Control visit every three month

Study Sites (1)

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