- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Seborrhea.
Displaying page 1 of 1.
EudraCT Number: 2006-005242-36 | Sponsor Protocol Number: K40-3 | Start Date*: 2006-12-13 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A multicenter, randomised, double-blind, placebo-controlled clinical study evaluating efficacy, safety and tolerability of topical K40 in 8 weeks treatment of adult patients with moderate to severe... | |||||||||||||
Medical condition: Seborrhoeic Dermatitis of the scalp. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006188-59 | Sponsor Protocol Number: K301-1 | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A multicenter, randomised double blind, placebo-controlled study of efficacy, safety and tolerability of Kaprolac® K301 for the treatment of seborrhoeic eczema (SE) of the scalp. | |||||||||||||
Medical condition: seborrhoeic dermatitis of the scalp | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000852-40 | Sponsor Protocol Number: TBSH-01 | Start Date*: 2012-08-03 | ||||||||||||||||
Sponsor Name:Dermal Laboratories | ||||||||||||||||||
Full Title: A double-blind, placebo-controlled study determining the efficacy of terbinafine shampoo in the treatment of pityriasis capitis and seborrhoeic dermatitis. | ||||||||||||||||||
Medical condition: The two severe dandruff conditions to be investigated in this study are pityriasis capitis and seborrhoeic dermatitis. | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005217-22 | Sponsor Protocol Number: RD.03.SPR.29079 | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Galderma Research & Development | |||||||||||||
Full Title: Efficacy and Safety of Clobetasol propionate shampoo 0.05% used in association with an antifungal shampoo in the treatment of moderate to severe Scalp Seborrheic Dermatitis | |||||||||||||
Medical condition: moderate to severe Scalp Seborrheic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001371-35 | Sponsor Protocol Number: S241-GB-03 | Start Date*: 2005-05-18 | |||||||||||
Sponsor Name:Stiefel Laboratories Maidenhead Ltd (commonly known as Stiefel Laboratories International Division) | |||||||||||||
Full Title: A Double-Blind, Placebo Controlled, Half-Head Design, CPO Solution Dose Ranging-Finding Study in Patients with Seborrhoeic Dermatitis of the Scalp | |||||||||||||
Medical condition: Seborrhoeic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013120-23 | Sponsor Protocol Number: 200802.2.45 | Start Date*: 2009-09-11 | |||||||||||
Sponsor Name:LABCATAL | |||||||||||||
Full Title: Efficacité et tolérance du LBC 45 dans la dermite séborrhéique du cuir chevelu | |||||||||||||
Medical condition: Dermite séborrhéique du cuir chevelu | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008353-35 | Sponsor Protocol Number: DC0115GM2012A | Start Date*: 2009-03-18 | |||||||||||
Sponsor Name:PIERRE FABRE DERMATOLOGIE REPRESENTED BY INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: EFFICACY STUDY OF A CICLOPIROXOLAMINE 1% FOAM (DC115 GM 02A) VERSUS CICLOPIROXOLAMINE 1.5% SHAMPOO (SEBIPROX®) IN THE TREATMENT OF MODERATE SEBORRHEIC DERMATITIS OF THE SCALP | |||||||||||||
Medical condition: Topical treatment of moderate seborrheic dermatitis of the scalp | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022861-93 | Sponsor Protocol Number: 201003.2.45 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:Laboratoire LABCATAL | |||||||||||||
Full Title: Confirmation de l'efficacité et de la tolérance du LBC 45 dans la dermite séborrhéique du cuir chevelu | |||||||||||||
Medical condition: Dermite séborrhéique du cuir chevelu | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003984-30 | Sponsor Protocol Number: CASM981N2203S | Start Date*: 2006-11-22 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, two-arm, vehicle-controlled, parallel-group, two stage study to evaluate and demonstrate the efficacy and to evaluate the safety of pimecrolimus 1% cream in... | |||||||||||||
Medical condition: Seborrhoeic Dermatitis (SD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000292-15 | Sponsor Protocol Number: S241-GB-10 | Start Date*: 2006-03-13 | |||||||||||
Sponsor Name:Stiefel Laboratories Maidenhead Ltd. | |||||||||||||
Full Title: A Phase II, Single-Centre, Randomised,Double-Blind, Parallel Group, CPO Solution, Dose Range Finding Study in Subjects with Seborrhoeic Dermatitis of the Scalp | |||||||||||||
Medical condition: Seborrhoeic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002060-26 | Sponsor Protocol Number: 1401201 | Start Date*: 2006-12-04 | |||||||||||
Sponsor Name:Intendis GmbH | |||||||||||||
Full Title: A double-blind, randomized, vehicle-controlled, 6-week exploratory multicenter pilot study of the efficacy and safety of Azelaic Acid (AzA) 15% gel in the topical treatment of mild to moderate seb... | |||||||||||||
Medical condition: Patients with mild to moderate seborrheic dermatitis of the facial area and meeting the specific eligibility criteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000720-19 | Sponsor Protocol Number: IDI01/2020 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:IDI FARMACEUTICI SRL | |||||||||||||
Full Title: A prospective, randomized, multicenter, open- label, two-arm and parallel-group Study to evaluate the efficacy and safety of Nicotinamide DS compared to Ciclopirox olamine cream at 1% in patients a... | |||||||||||||
Medical condition: Patients affected by seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003106-41 | Sponsor Protocol Number: CHDR1733 | Start Date*: 2018-09-05 | |||||||||||
Sponsor Name:Maruho Co., Ltd. | |||||||||||||
Full Title: A phase 2, randomized, vehicle and ketoconazole-controlled, evaluator-blinded, study to explore the efficacy, pharmacodynamics and safety of omiganan 1.75% topical gel BID in patients with mild to ... | |||||||||||||
Medical condition: Mild to moderate facial seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004649-14 | Sponsor Protocol Number: ASF-1057-303 | Start Date*: 2008-02-19 |
Sponsor Name:Astion Pharma A/S | ||
Full Title: Safety of ASF 1057 cream 0.5% under long term use in the treatment of seborrhoeic dermatitis: A 12 month open label extension multi-centre phase III trial | ||
Medical condition: Seborrhoeic dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) FI (Completed) | ||
Trial results: (No results available) |
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: 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 |
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