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Kusajili – Clinical trials directory
Result
of your search per sponsor: Claire L Shovlin
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Case Notes Review on Patients With Hereditary Haemorrhagic Telangiectasia
The Hammersmith Hospital provides a clinical service for patients with Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations that is unique in the United Kingdom...
Country
United Kingdom
organs
None
Specialty
None
Opened trial
More information
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Cardiopulmonary Exercise Testing to Evaluate Pulmonary AVMs
Pulmonary arteriovenous malformations (PAVMs) are a rare vascular condition affecting the lungs. PAVMs lead to low blood oxygen levels, yet are very well tolerated by patients. This study ...
Country
None
organs
None
Specialty
None
Opened trial
More information
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Study of Histological Samples From Patients With Hereditary Haemorrhagic Telangiectasia
Hereditary Haemorrhagic Telangiectasia (HHT, also known as Osler-Weber-Rendu Syndrome) is an disease that leads to the development of dilated and fragile blood vessels. We propose to obtai...
Country
United Kingdom
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Molecular Studies on Hereditary Haemorrhagic Telangiectasia Families
Hereditary haemorrhagic telangiectasia is a disease inherited as an autosomal dominant disease. Analysing DNA from affected and unaffected family members allows us to identify the location...
Country
None
organs
None
Specialty
None
Opened trial
More information
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Study of Endothelial Cells in Patients With Hereditary Haemorrhagic Telangiectasia
Hereditary Haemorrhagic Telangiectasia (HHT, also known as Osler-Weber-Rendu Syndrome) is an disease that leads to the development of dilated and fragile blood vessels. We propose to cultu...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Claire L Shovlin, PhD FRCP
Update Il y a 4 ans
Diet and Hereditary Haemorrhagic Telangiectasia
Hereditary Haemorrhagic Telangiectasia (HHT) affects 1 in 5,000 people. The purpose of this study is to provide data regarding the diet and nosebleed frequency using a questionnaire. This...
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Claire L Shovlin, PhD MA MB BChir FRCP
Update Il y a 4 ans
Hereditary Haemorrhagic Telangiectasia Flight Safety Study
Hereditary Haemorrhagic Telangiectasia (HHT) is a condition in which sufferers have abnormal blood vessels which makes them more likely to bleed than other people, particularly in the lung...
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Claire L Shovlin, PhD MA MB BChir FRCP
Update Il y a 4 ans
The Efficacy and Safety of Iron Supplementation
Each year, 5 million packs of iron tablets are dispensed in England and Wales to treat anaemia due to iron deficiency. Iron tablets are not always easy to take. The investigators think tha...
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Claire L Shovlin, PhD FRCP
Update Il y a 4 ans
Cardiopulmonary Exercise Testing to Evaluate Pulmonary AVMs With and Without Airflow Obstruction
Pulmonary arteriovenous malformations (PAVMs) are a rare vascular condition affecting the lungs. PAVMs lead to low blood oxygen levels, yet are very well tolerated by patients. This study ...
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Claire L Shovlin
Update Il y a 4 ans
Studies of White Blood Cells Derived From HHT Patients
Hereditary Haemorrhagic Telangiectasia (HHT, also known as Osler-Weber-Rendu Syndrome) is an disease that leads to the development of dilated and fragile blood vessels. We propose to take ...
Country
None
organs
None
Specialty
None
unknown
More information
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