- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
8 result(s) found for: Angiomas.
Displaying page 1 of 1.
EudraCT Number: 2013-005199-17 | Sponsor Protocol Number: IIBSP-TIM-2013-156 | Start Date*: 2014-07-16 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: Efficacy and safety of topical administration of timolol maleate 0.5% solution in the treatment of Child Proliferative Hemangioma Early Stage Surface. Randomized Controlled Study | ||
Medical condition: Children Superficial Hemangioma | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000202-36 | Sponsor Protocol Number: CHUBX 2007/27 | Start Date*: 2008-06-12 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Etude clinique randomisée du propranolol versus placebo dans le traitement des hémangiomes capillaires infantiles. | |||||||||||||
Medical condition: Hémangiomes capillaires | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018102-22 | Sponsor Protocol Number: V00400SB102 | Start Date*: 2010-03-26 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE | |||||||||||||
Full Title: A multicentre, open-label, repeated-dose, pharmacokinetic study of Propranolol in infants treated for proliferating infantile hemangiomas (IHs) requiring systemic therapy. | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023488-16 | Sponsor Protocol Number: V00400SB301 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE represented by INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: A multicentre, open-label study of propranolol in infants with proliferating infantile hemangioma requiring systemic therapy | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019754-41 | Sponsor Protocol Number: PROHÄM | Start Date*: 2010-10-19 | |||||||||||
Sponsor Name:InfectoPharm Arzneimittel und Consilium GmbH | |||||||||||||
Full Title: Multizentrische, prospektive, einarmige Phase III-Studie zur Wirksamkeit und Sicherheit einer oralen Therapie mit Propranolol (ProAngiol Saft; 2 mg/kg KG/d mit fakultativer Dosiserhöhung auf 3 mg/k... | |||||||||||||
Medical condition: Hemangioma in infants and toddlers, requiring systemic therapy | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005555-80 | Sponsor Protocol Number: V00400SB302 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie represented by IRPF | |||||||||||||
Full Title: Efficacy and safety of Hemangiol solution in the treatment of high risk infantile hemangioma. A Multinational Single Arm Study | |||||||||||||
Medical condition: High risk infantile haemangioma | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013262-84 | Sponsor Protocol Number: V00400SB201 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE | |||||||||||||
Full Title: A randomised, controlled, multidose, multicentre, adaptive phase II/III study in infants with proliferating infantile hemangiomas requiring systemic therapy to compare four regimens of propranolol ... | |||||||||||||
Medical condition: Proliferating Infantile Hemangioma | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Completed) HU (Completed) LT (Completed) CZ (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012115-18 | Sponsor Protocol Number: IMP13617 | Start Date*: 2010-03-22 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Primovist enhanced MRI for the detection and evaluation of focal liver lesions | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: All benign and malignant focal liver lesions e.g. colorectal liver metastases, HCC, haemangioma, adenoma, cysts, FNH. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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