- Trials with a EudraCT protocol (341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (39)
341 result(s) found for: Eczema.
Displaying page 1 of 18.
EudraCT Number: 2009-011931-11 | Sponsor Protocol Number: H 552 000 - 0911 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Almirall Hermal GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Explorative, double-blind, randomized, controlled multi-center phase II study to evaluate the efficacy and safety of topically applied combinational product LAS41003 once daily versus corresponding... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients aged 18 and older suffering from at least one clinically diagnosed superinfected or impetiginised eczema such as e.g. • superinfected or impetiginised atopic eczema • superinfected or impe... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021284-33 | Sponsor Protocol Number: protocoltwo17.12.09. | Start Date*: 2010-10-07 | ||||||||||||||||||||||||||
Sponsor Name:Research and Development Department, John Radcliffe Hospital | ||||||||||||||||||||||||||||
Full Title: Proof of concept study of combined allergen immunotherapy and antibiotics for the treatment of chronic atopic eczema | ||||||||||||||||||||||||||||
Medical condition: Severe chronic atopic eczema | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004432-20 | Sponsor Protocol Number: ACE-ATOPI-1 | Start Date*: 2008-09-03 | |||||||||||
Sponsor Name:ACE Aps | |||||||||||||
Full Title: Efficacy and tolerability of captopril oinment 0,1% og 0,3% in atopic dermatitis. A randomised, double-blind, placebocontrolled, doseescalating, intra-individual clinical study. | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004443-22 | Sponsor Protocol Number: Spirig I 04-05 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Spirig Pharma AG | |||||||||||||
Full Title: Untersuchung der Wirksamkeit einer glycerinhaltigen Creme bei der Behandlung von Atopischer Dermatitis. Kontrolliert, randomisierte Doppel-Blind-Studie. | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002926-23 | Sponsor Protocol Number: RV2478B 03 LT 301 100 MVC | Start Date*: 2004-12-22 | |||||||||||
Sponsor Name:INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: Evaluation of the impact of the moisturizing milk RV2478B on the use of corticoids and on quality of life, in a population of children with atopic dermatitis. | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006982-17 | Sponsor Protocol Number: 05.09.2006 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:Division of Special and Environmental Dermatology | |||||||||||||
Full Title: UVA 1 therapy versus 5-MOP UVA photochemotherapy for patients with severe generalized atopic dermatitis | |||||||||||||
Medical condition: Severe generalized atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000984-34 | Sponsor Protocol Number: 6630-9170-917016 | Start Date*: 2018-05-24 | |||||||||||||||||||||
Sponsor Name:Medice Arzneimittel Pütter GmbH & Co KG | |||||||||||||||||||||||
Full Title: A multi-center, randomized, double-blind, phase II trial with intraindividual comparison to assess superiority of Soventol HydroCortisonACETAT 1 % Cremogel versus vehicle on lesional skin in patien... | |||||||||||||||||||||||
Medical condition: atopic dermatitis, seborrheic eczema or stasis dermatitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000715-25 | Sponsor Protocol Number: 6520-9170-07 | Start Date*: 2013-07-23 | |||||||||||||||||||||
Sponsor Name:MEDICE Arzneimittel Pütter GmbH & Co.KG | |||||||||||||||||||||||
Full Title: A multi-center, randomized, double-blind, phase II trial with intraindividual comparison to assess superiority of Soventol HydroCort 1% cream versus vehicle on lesional skin in patients with mild a... | |||||||||||||||||||||||
Medical condition: manifest atopic dermatitis diagnosed according to Hanifin and Rajka, or seborrheic eczema or stasis dermatitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003001-26 | Sponsor Protocol Number: 2009 | Start Date*: 2013-12-23 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: Choice Of Moisturiser in Eczema Treatment (COMET): A feasibility study of pragmatic, single blind, randomised clinical trial to compare the clinical and cost effectiveness of leave-on emollients in... | |||||||||||||
Medical condition: Eczema | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003485-25 | Sponsor Protocol Number: V00034 CR 402 1B | Start Date*: 2008-10-01 | |||||||||||
Sponsor Name:Pierre Fabre Médicament | |||||||||||||
Full Title: Impact of the V0034CR 01B emollient on atopic dermatitis symptoms in children. A randomised, placebo-controlled, parallel-groups, double-blind study | |||||||||||||
Medical condition: Children between 2 and 7 years, presenting with atopic dermatitis according to the diagnostic criteria of the UK Working party and whose IGA score is < or = 1 at inclusion. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) FR (Completed) EE (Completed) DE (Completed) PL (Completed) LV (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003667-31 | Sponsor Protocol Number: TUD_PROVE_001 | Start Date*: 2007-03-30 | |||||||||||
Sponsor Name:Medical Faculty, TU Dresden | |||||||||||||
Full Title: Prednisolone vs. Ciclosporine in Severe Atopic Eczema. PROVE - Study | |||||||||||||
Medical condition: atopic eczema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003406-31 | Sponsor Protocol Number: CCMK389B12201 | Start Date*: 2021-01-10 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, subject and investigator blinded, placebo-controlled multicenter study to assess the efficacy and safety of CMK389 in patients with moderate to severe atopic dermatitis | |||||||||||||
Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) FR (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003644-59 | Sponsor Protocol Number: CASM981CDE17 | Start Date*: 2006-11-21 | |||||||||||
Sponsor Name:University of Heidelberg | |||||||||||||
Full Title: A two months study of the utility of Elidel cream 1% (pimecrolimus) in the long term management of atopic hand eczema. | |||||||||||||
Medical condition: chronically relapsing atopic hand eczema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003066-34 | Sponsor Protocol Number: 101-PG-PSC-150 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: A randomized, double blinded, placebo controlled multicenter study for the efficacy and safety of Depigoid® House dust mites (HDM) in patients suf-fering from moderate to severe atopic eczema. | |||||||||||||
Medical condition: Moderate to severe atopic eczema with or without rhinitis and/or rhinoconjunctivitis caused by clinical relevant IgE-mediated sensitization against House dust mites (HDM) leading to aggravation of ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001488-79 | Sponsor Protocol Number: HCP 20A | Start Date*: 2005-05-05 | |||||||||||
Sponsor Name:Healthcare Product Development | |||||||||||||
Full Title: HCP 20A for the treament of atopic eczema: A pilot study to investigate the clinical efficacy of a novel treatment for eczema incorporating anti-inflammatory and antibacterial agents. | |||||||||||||
Medical condition: Eczema | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003591-37 | Sponsor Protocol Number: SPON846-10 | Start Date*: 2012-09-03 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: Children with Eczema Antibiotic Management Study (CREAM) | |||||||||||||
Medical condition: Atopic Eczema | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000688-34 | Sponsor Protocol Number: 2738 | Start Date*: 2017-06-12 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: The Best Emollient for Eczema (BEE) trial: a randomised trial comparing the effectiveness of four commonly prescribed emollients for children with eczema | |||||||||||||
Medical condition: Eczema | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002477-23 | Sponsor Protocol Number: FG-506-06-FR-04 | Start Date*: 2005-04-01 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: Comparative, multicentre, randomised, double-blind study to assess the efficacy of tacrolimus 0.1% ointment versus fluticasone 0.005% ointment in adult patients suffering from moderate to severe at... | |||||||||||||
Medical condition: Moderate to severe atopic dermatitis and presenting with so-called "red face" lesions of the head and neck. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005890-37 | Sponsor Protocol Number: K201-I/280301BS | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: Assessment of the effects on barrier impairment, clinical features and bacterial colonization of topical formulations in patients with atopic eczema; a phase IIa, single-center, randomized, observe... | |||||||||||||
Medical condition: To assess the barrier impairment, clinical skin condition and bacterial colonization in patients with atopic eczema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002571-42 | Sponsor Protocol Number: 310409BS | Start Date*: 2011-11-29 | |||||||||||
Sponsor Name:GALENpharma GmbH | |||||||||||||
Full Title: Phase IIa, multi-center, randomized, double-blind, vehicle-controlled study for assessment of clinical skin condition and effects on barrier impairment of a topical formulation containing tarenflur... | |||||||||||||
Medical condition: Subjects with mild to moderate atopic eczema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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