- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
58 result(s) found for: Telangiectasia.
Displaying page 1 of 3.
EudraCT Number: 2017-003272-31 | Sponsor Protocol Number: NL.EPITRAC.0107.17 | Start Date*: 2018-05-18 | ||||||||||||||||
Sponsor Name:St. Antonius Ziekenhuis | ||||||||||||||||||
Full Title: Efficacy and safety of oral itraconazole in the reduction of epistaxis severity in hereditary hemorrhagic telangiectasia | ||||||||||||||||||
Medical condition: Severe epistaxis in patients with Hereditary Hemorrhagic Telangiectasia also known as Rendu-Osler-Weber disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003982-24 | Sponsor Protocol Number: HHT-HOPE-2016 | Start Date*: 2017-03-16 | |||||||||||
Sponsor Name:Asociación HHT España | |||||||||||||
Full Title: A phase IV-II, single-center, open, single arm treatment, low level of intervention, to assess the efficacy clinical trial and safety of intranasal administration of ethamsylate in the treatment of... | |||||||||||||
Medical condition: Hereditary hemorrhagic telangiectasia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004096-36 | Sponsor Protocol Number: THALI-HHT | Start Date*: 2011-10-11 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Efficacy of thalidomide in the treatment of severe recurrent epistaxis in hereditary hemorrhagic telangiectasia (HHT) | |||||||||||||
Medical condition: Severe recurrent epistaxis in hereditary hemorrhagic telangiectasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004010-26 | Sponsor Protocol Number: THR-317-003 | Start Date*: 2018-08-03 | |||||||||||
Sponsor Name:ThromboGenics NV | |||||||||||||
Full Title: A Phase 2, open-label, multi-centre study to assess the efficacy and safety of intravitreal THR-317 for the treatment of macular telangiectasia Type 1 (MacTel 1) | |||||||||||||
Medical condition: Macular Telangiectasia Type 1 (MacTel 1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004789-27 | Sponsor Protocol Number: 21.November.2015 | Start Date*: 2016-03-03 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Topical brimonidine to reduce post-inflammatory response after IPL- treatment and effect on IPL-efficacy in patients with facial telangiectasias | |||||||||||||
Medical condition: Inflammation after IPL-treatment in patients with facial telangiectasias | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022315-19 | Sponsor Protocol Number: IEDAT-ERY01-2010 | Start Date*: 2011-01-11 | |||||||||||
Sponsor Name:ERYDEL S.P.A. | |||||||||||||
Full Title: Valutazione degli effetti del Desametasone Sodio Fosfato Intra-Eritrocitario sui Sintomi Neurologici in Pazienti con Atassia Teleangectasia | |||||||||||||
Medical condition: Patients with Ataxia-Teleangectasia (AT) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000385-55 | Sponsor Protocol Number: 69HCL15_0063 | Start Date*: 2015-05-12 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: TEMPO : Efficacité du TIMOLOL en administration nasale pour le traitement des épistaxis dans la maladie de Rendu-Osler. Essai randomisé en double insu contre placebo | |||||||||||||
Medical condition: Rendu-Osler disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004204-19 | Sponsor Protocol Number: 2013-827 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Efficacité du bevacizumab en spray nasal pour le traitement des épistaxis dans la maladie de Rendu-Osler | |||||||||||||
Medical condition: Rendu-Osler disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000338-36 | Sponsor Protocol Number: IEDAT-03-2018 | Start Date*: 2018-05-31 | |||||||||||
Sponsor Name:EryDel S.p.A. | |||||||||||||
Full Title: Open-label, Long-term, Extension Treatment using Intra-Erythrocyte Dexamethasone Sodium Phosphate in Patients with Ataxia Telangiectasia Who Participated in the IEDAT-02-2015 Study | |||||||||||||
Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) NO (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005241-31 | Sponsor Protocol Number: IEDAT-02-2015 | Start Date*: 2016-09-14 | |||||||||||
Sponsor Name:EryDel S.p.A. | |||||||||||||
Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Effects of Intra-Erythrocyte Dexamethasone Sodium Phosphate on Neurological Symptoms in Patients with Ataxia Telan... | |||||||||||||
Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) NO (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006233-40 | Sponsor Protocol Number: CRFB002ADE04 | Start Date*: 2007-08-06 | |||||||||||
Sponsor Name:Department of Ophthalmology, Bonn University | |||||||||||||
Full Title: Ranibizumab in idiopathic macular telangiectasia, type2 A prospective interventional non-randomized study comparing the efficacy and safety of intravitreal ranibizumab (dosing regimen 0.5mg every ... | |||||||||||||
Medical condition: Typical findings in Type 2 idiopathic macular telangiectasia (type2-IMT)are parafoveal ectatic capillaries, The disease is characterized by a slow decrease in visual acuity, reading difficulties an... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006755-44 | Sponsor Protocol Number: 2008-510 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
Full Title: METAFORE : Maladie de Rendu-Osler : Etude de l’Efficacité et de la tolérance du Bevacizumab utilisé pour le traitement des formes hépatiques sévères. Etude de phase II | |||||||||||||
Medical condition: Maladie de Rendu-Osler | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004539-57 | Sponsor Protocol Number: Dio/01/2013 | Start Date*: 2014-01-30 | ||||||||||||||||
Sponsor Name:ALIO MEDICA Sp. z o.o. | ||||||||||||||||||
Full Title: A phase III, double-blind, placebo-controlled, randomized, three-arm parallel, study assessing efficacy and safety of 4 months of diosmin administration for the treatment of lower extremity teleang... | ||||||||||||||||||
Medical condition: lower extremity teleangiectasias and gynoid lipodystrophy (edematous fibrosclerotic panniculopathy commonly known as cellulite) | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004122-70 | Sponsor Protocol Number: 04M107 | Start Date*: 2005-11-15 |
Sponsor Name:Great Ormond Street Hospital | ||
Full Title: Immunogenicity of conjugate pneumococcal vaccine (Prevenar) in patients with ataxia -telangiectasia (AT) including a randomised study of one versus two doses of vaccine. | ||
Medical condition: Ataxia Telangiectasia (AT) is a genetic condition in which there is a deficiency of the immune system with excessive susceptibility to pneumonia and other infections. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003585-40 | Sponsor Protocol Number: NL.TACRO.10.7.19 | Start Date*: 2019-12-17 | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: An uncontrolled, open label pilot-study assessing the efficacy in reducing bleeding severity, and the safety of oral tacrolimus in patients with hereditary hemorrhagic telangiectasia | |||||||||||||
Medical condition: Gastrointestinal bleeding and epistaxis caused by hereditary hemorrhagic telangiectasia. Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant inherited disease characterized by muco... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004179-11 | Sponsor Protocol Number: 2018-4898 | Start Date*: 2019-06-03 |
Sponsor Name:Radboudumc | ||
Full Title: Effectiveness of Somatostatin Analogues in Patients with hereditary hemorrhagic telangiectasia and symptomatic gastrointestinal bleeding, the SAIPAN-trial: a multicenter, randomized, open-label, pa... | ||
Medical condition: Hereditary hemorrhagic telangiectasia (HHT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Ongoing) FR (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003260-12 | Sponsor Protocol Number: NTMT-03-B | Start Date*: 2018-10-02 |
Sponsor Name:Neurotech Pharmaceuticals Inc. | ||
Full Title: A Phase 3 Multicenter Randomized, Sham-Controlled Study to Determine the Safety and Efficacy of NT-501 in Macular Telangiectasia type 2 | ||
Medical condition: Macular Telangiectasia type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001031-39 | Sponsor Protocol Number: 69HCL17_0018 | Start Date*: 2017-05-19 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: BABH Study: Efficacy and safety of bevacizumab on severe bleedings associated with Hemorrhagic Hereditary Telangiectasia (HHT). A National, randomized multicenter phase III study. | |||||||||||||
Medical condition: Hemorrhagic Hereditary Telangiectasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003234-82 | Sponsor Protocol Number: NTMT-03-A | Start Date*: 2018-06-13 |
Sponsor Name:Neurotech Pharmaceuticals | ||
Full Title: A Phase III Multicenter Randomized, Sham Controlled, Study to Determine the Safety and Efficacy of Renexus® in Macular Telangiectasia type 2 | ||
Medical condition: Macular Telangiectasia type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004407-39 | Sponsor Protocol Number: IB1001-203 | Start Date*: 2019-09-18 |
Sponsor Name:IntraBio Ltd. | ||
Full Title: Effects of N-Acetyl-L-Leucine on Ataxia-Telangiectasia (A-T): A multinational, multicenter, open-label, rater-blinded Phase II study. | ||
Medical condition: To demonstrate that N-Acetyl-L-Leucine is effective in improving symptoms, functioning, and quality of life in patients with Ataxia-Telangiectasia (A-T) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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