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CompletedNCT00733655

Study of Histological Samples From Patients With Hereditary Haemorrhagic Telangiectasia

Histological Samples From Patients With Hereditary Haemorrhagic Telangiectasia

Status
Completed
Phase
Study type
Observational
Enrollment
6 (actual)
Sponsor
Imperial College London · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

In this study the investigators will obtain histological samples from people with hereditary haemorrhagic telangiectasia (HHT, also known as Osler-Weber-Rendu Syndrome).

Detailed description

HHT is an inherited condition that leads to the development of dilated and fragile blood vessels. We propose to obtain small skin samples from patients with HHT in order to analyze the samples using histological methods, and study the properties of vascular endothelial cells derived from patients. We hypothesize that these cells will show differences when compared to normal endothelial cells, which may be confirmed in single time point analyses in histological samples. We anticipate that that these findings may help to explain aspects of the HHT disease phenotype.

Conditions

Timeline

Start date
2008-09-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2008-08-13
Last updated
2023-09-28

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00733655. Inclusion in this directory is not an endorsement.

Study of Histological Samples From Patients With Hereditary Haemorrhagic Telangiectasia (NCT00733655) · Clinical Trials Directory