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Telangiectasis clinical trials

View clinical trials related to Telangiectasis.

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NCT ID: NCT04148950 Completed - Clinical trials for Varicose Veins of Lower Limb

Effects of Kinesio Taping Method on Functional Capacity and Quality of Life in Patients With Chronic Venous Disease

Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this randomised and controlled study is to investigate the effects of Kinesio Taping method and compression stockings, combined with exercise therapy, on pain, edema, functional capacity and quality of life in patients with chronic venous disease. Therefore, the study compares effectiveness of these two methods for chronic venous disease.

NCT ID: NCT04139018 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Timolol Gel for Epistaxis in Hereditary Hemorrhagic Telangiectasia

ETIC-HHT
Start date: October 20, 2019
Phase: Phase 2
Study type: Interventional

This study is a double-blinded, randomized controlled trial to evaluate the efficacy of an intranasal topical timolol gel in the care for epistaxis in adults with hereditary hemorrhagic telangiectasia.

NCT ID: NCT04132323 Completed - Sclerotherapy Clinical Trials

Low Concentrate Detergents Versus Hypertonic Glucose for the Treatment of Telangiectasia

Start date: October 25, 2019
Phase: N/A
Study type: Interventional

Using of low concentrate sodium tetradecyl sulfate for sclerotherapy of telangiectasias should be no less effective than hypertonic glucose, and have a comparable frequency of adverse events.

NCT ID: NCT04113187 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Propranolol for Epistaxis in Hereditary Hemorrhagic Telangiectasia Patients

EPERO
Start date: June 23, 2020
Phase: Phase 3
Study type: Interventional

Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic disorder of angiogenesis associated with disabling epistaxis. Management of these nose bleedings requires more effective treatment. Propranolol, a beta-blocker, is a potentially useful therapeutic considering its anti-angiogenic properties. Our objective is to explore the efficacy of propranolol, three months after its introduction, on the cumulative duration of epistaxis in HHT patients.

NCT ID: NCT04108052 Completed - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

Diagnostic Value of Ultra-low Dose Thoracic Scanner for the Pulmonary Arteriovenous Malformation Detection in HHT Patient

ULD OSLER
Start date: November 28, 2019
Phase: N/A
Study type: Interventional

Hereditary hemorrhagic telangiectasia (HHT) is linked to a dysregulation of angiogenesis leading to the formation of arteriovenous malformations (AVM): cutaneo-mucous telangiectasia and visceral shunts. The diagnosis is clinical and based on Curaçao criteria: recurrent epistaxis, cutaneo-mucous telangiectasia, hereditary signs and presence of visceral AVM. Pulmonary AVMs (PAVM) expose patients to many potentially life-threatening complications, such as strokes or brain abscesses due to the right-left shunt created and the lack of filtration barrier of the pulmonary capillary within the AVM. These patients should therefore have regular monitoring throughout their life by a chest CT scanner every 5 to 10 years in the absence of PAVM at the initial scan or more often if PAVMs are present. The management of PAVMs is based on their early detection and embolization in interventional radiology during which is set up within the afferent artery of the PAVM an embolizing agent, the coil. However, the risk of cumulative irradiation exposure from thoracic scanners and repeated thoracic embolizations over time could be reduces by a decrease of X-rays dose. A new thoracic CT imaging protocol validated in the United States in the primary screening of lung cancer, the ultra-low dose protocol, is a CT scanner acquired at an irradiation dose equivalent to that of a frontal chest x-ray and in profile. The dose reduction is of 40 times the usual dose of a chest CT scanner. The lung parenchyma has a high natural contrast on thoracic CT images and there are few adjacent attenuating structures allowing a drastic reduction of dose. However, from this dose, the image quality is degraded with an increase of the image noise. The diagnostic performances have to be confirmed with qualitative and quantitative measurements. Thus, the objective of this study is to compare the sensitivity and the specificity of the current scanner and the ultra-low dose scanner to reduce the exposure to X-rays.

NCT ID: NCT04037189 Recruiting - Lymphoma Clinical Trials

Treatment of Leukemia and Lymphoma in Children With Ataxia Telangiectasia

Start date: July 28, 2019
Phase:
Study type: Observational

Ataxia telangiectasia (A-T) is a multisystem disease with diverse manifestations, including progressive neurodegeneration, immunodeficiency, respiratory disease, and genomic instability. One of the most important features of A-T is the increased predisposition to cancer, especially to lymphoid malignancies. Patients with A-T are generally excluded from collaborative clinical trials, their treatment outcomes and toxicity profiles have rarely been reported, and little is currently known concerning the treatment intensity required to provide a reasonable balance between efficacy and toxicity. The aims of this study are to build a large international de-identified database of children with A-T treated for leukemia and lymphoma, to investigate epidemiology and outcome of treatment, toxicity profiles and risk factors which impact outcome, in order to eventually enable the generation of data-based treatment recommendations for this population.

NCT ID: NCT04004728 Completed - Leg Veins Clinical Trials

Laser Treatment Of Leg Telangiectasias

Start date: March 2010
Phase: N/A
Study type: Interventional

Is 1064 nm YAG Laser better than sclerotherapy to treat leg veins?

NCT ID: NCT03981562 Recruiting - Clinical trials for Hereditary Haemorrhagic Telangiectasia

Vitamin D and Hereditary Haemorrhagic Telangiectasia

Start date: July 16, 2018
Phase: Phase 2
Study type: Interventional

The study aims to assess whether supplementing vitamin D in patients diagnosed with Hereditary Haemorrhagic Telangiectasia (HHT) will decrease the frequency and severity of nosebleeds these patients experience. It is hypothesized that the larger the dose of daily vitamin D given to the patients, the less frequent and less severe the nosebleeds will be.

NCT ID: NCT03962114 Completed - Clinical trials for Ataxia Telangiectasia

Effects of Vitamin B3 in Patients With Ataxia Telangiectasia

Start date: March 18, 2019
Phase: Phase 2
Study type: Interventional

This clinical trial investigates the effects of nicotinamide riboside (vitamin B3) on the disease course of patients with ataxia telangiectasia. Patients will be treated during four consecutive months with nicotinamide riboside (25mg/kg/day), followed by a washout period of two months. Main study parameters/endpoints: Ataxia, dysarthria, quality of life, laboratory parameters.

NCT ID: NCT03954782 Completed - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

Efficacy of Nintedanib Per os as a Treatment for Epistaxis in HHT Disease.

EPICURE
Start date: June 22, 2020
Phase: Phase 2
Study type: Interventional

The recognized manifestations of HHT are all due to abnormalities in vascular structure. Epistaxis are spontaneous, very variable, may occur as often as several times every day, and are recurrent in 90% of patients and associated with chronic and severe anemia in 2-10%. They also significantly reduce quality of life. Blood transfusions are sometimes required in 10-30% of patients. Previous studies showed that antiangiogenic treatments such as anti-VEGF treatment (bevacizumab) administered intravenously was efficient on epistaxis and dramatically reduced nosebleeds. Tyrosine kinase inhibitors are anti-angiogenic molecules which are available orally and could therefore overcome the difficulties encountered with bevacizumab. The investigator hypothesized that nintedanib, acting by indirect inhibition of the VEGF receptor should allow a reduction of epistaxis in HHT patient. Nintedanib has been used in one HHT patient following the diagnosis of Insterstitial Pulmonary Fibrosis (published case report in 2017, Kovacs et al) with encouraging results. The aim is to evaluate efficacy of nintedanib for the treatment of epistaxis in HHT patients