- Trials with a EudraCT protocol (244)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (20)
244 result(s) found for: Scalp.
Displaying page 1 of 13.
EudraCT Number: 2022-000797-26 | Sponsor Protocol Number: IM011-220 | Start Date*: 2023-01-19 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A PHASE 3B/4, MULTICENTER, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF DEUCRAVACITINIB IN PARTICIPANTS WITH MODERATE-TO-SEVERE SCALP PSORIASIS (PSORIATY... | |||||||||||||
Medical condition: Moderate-to-severe Scalp Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2005-002864-27 | Sponsor Protocol Number: MBL 0503 INT | Start Date*: 2005-10-07 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to DAIVONEX/DOVONEX Scalp Solution in Patients with Scalp Psoriasis. A phase III study comparing a gel containing calcipotriol 50 mcg/g plu... | |||||||||||||
Medical condition: Psoriasis of the scalp Clinical signs of psoriasis vulgaris on trunk and/or limbs, or earlier diagnosed with psoriasis vulgaris on trunk and/or limbs Extent of scalp psoriasis involving 10% or more... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003354-92 | Sponsor Protocol Number: ARQ-154-204 | Start Date*: 2020-05-12 | |||||||||||
Sponsor Name:Arcutis Biotherapeutics, Inc. | |||||||||||||
Full Title: A Phase 2b, 8-Week, Parallel Group, Double Blind, Vehicle-Controlled Study of the Safety and Efficacy of ARQ-154 Foam 0.3% Administered QD in Adolescents and Adults with Scalp and Body Psoriasis | |||||||||||||
Medical condition: Scalp and Body Plaque Psoriasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002152-33 | Sponsor Protocol Number: MBL 0406 INT | Start Date*: 2004-11-12 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to Calcipotriol in the Gel Vehicle and Betamethasone Dipropionate in the Gel Vehicle in Scalp Psoriasis. A phase III study comparing a gel ... | |||||||||||||
Medical condition: Scalp psoriasis with 10% involvement of the scalp | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) IE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001106-42 | Sponsor Protocol Number: 16-01/CalciBet-Gel | Start Date*: 2016-09-19 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomised clinical study comparing efficacy and safety of Calcipotriol 50 µg/g_Betamethasone 0.5 mg/g Gel (Test) vs. Daivobet(R) Gel (Reference) vs. Vehicle in patients with scalp ps... | |||||||||||||
Medical condition: Psoriasis capitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 2009-016261-28 | Sponsor Protocol Number: H 521 000 - 0915 | Start Date*: 2010-01-26 | ||||||||||||||||
Sponsor Name:Almirall Hermal GmbH | ||||||||||||||||||
Full Title: Randomized, observer-blind, multi-center, reference-controlled phase IIb study to evaluate the efficacy of topically applied LAS41002 lotion in the treatment of scalp psoriasis | ||||||||||||||||||
Medical condition: Psoriasis vulgaris on the scalp | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002015-86 | Sponsor Protocol Number: MBL 0405 INT | Start Date*: 2004-11-03 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to Betamethasone Dipropionate in the Gel Vehicle, Calcipotriol in the Gel Vehicle and the Gel Vehicle alone in Scalp Psoriasis. | |||||||||||||
Medical condition: Psoriasis of the scalp. Extent: Minimum 10% of the total scalp area. Disease severity: Graded as "moderate", "severe" or "very severe" according to the investigator´s global assessment of disease s... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007088-25 | Sponsor Protocol Number: V00071 GM 201 1A | Start Date*: 2008-04-15 |
Sponsor Name:Pierre Fabre Dermatologie | ||
Full Title: Efficacy and tolerance of V0071 GM 01A in inflammatory seborrhoeic dermatitis of the scalp. | ||
Medical condition: Inflammatory seborrhoeic dermatitis of the scalp in adult | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (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: 2019-000215-92 | Sponsor Protocol Number: BYH1003 | Start Date*: 2019-07-02 | |||||||||||
Sponsor Name:Bay Pharma GmbH | |||||||||||||
Full Title: Prospective, randomized, double blinded, placebo controlled, multicentre study for the evaluation of efficacy and safety of a Tacrolimus-containing solution (TACRO-Skin) in subjects with mild to se... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002861-19 | Sponsor Protocol Number: MBL 0407 INT | Start Date*: 2005-01-24 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Long-term treatment of Scalp Psoriasis with Calciptriol plus Betamethasone dipropionate gel. A phase III safety study of a new gel containing calcipotriol 50mcg/g plus betamethasone 0.5 mg/g (as di... | |||||||||||||
Medical condition: Psoriasis of the scalp Extent: Minimum 10% of the total scalp area Disease severity: Graded as "moderate", "severe", or "very severe" according to the investigator's global assessment of disease se... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005085-21 | Sponsor Protocol Number: KCSA-03 | Start Date*: 2005-12-13 |
Sponsor Name:Dermal Laboratories Limited | ||
Full Title: Scalp lotion for the treatment of pityriasis capitis (severe dandruff) and seborrhoeic dermatitis. | ||
Medical condition: Seborrhoeic dermatitis and pityriasis capitis of the scalp. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005288-29 | Sponsor Protocol Number: P1204LT | Start Date*: 2013-06-07 | |||||||||||
Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
Full Title: A single-center randomized, active-controlled, observer-blinded, parallel group trial to evaluate the efficacy and safety of a topical dimeticone formulation (Loion®) compared to 10% saliclylic aci... | |||||||||||||
Medical condition: psoriatic plaques in patients with chronic psoriasis capitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000379-15 | Sponsor Protocol Number: 192024-057 Amendment 2 | Start Date*: 2011-06-21 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Parallel-group Study to Evaluate the Safety and Efficacy of Bimatoprost Solution 0.03%, 0.1%, and 0.3% Compared with Vehicle in Men with Androgenic Alopecia... | |||||||||||||
Medical condition: Androgenic alopecia in men | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003073-27 | Sponsor Protocol Number: RD.03.SPR29064 | Start Date*: 2007-02-06 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject preference comparison between Clobetasol propionate shampoo, 0.05% and three other topical corticosteroids in the treatment of moderate to severe Scalp psoriasis | |||||||||||||
Medical condition: Moderate to Severe Scalp Psoriasis with a Global Severity Score of 3 at least on a scale from 0 to 5. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004860-78 | Sponsor Protocol Number: P1209NY | Start Date*: 2014-05-09 | |||||||||||
Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
Full Title: A randomised, active-controlled, observer-blind, non-inferiority study to investigate the efficacy, safety and tolerability of a local treatment with dimeticone-based pediculicides in head lice inf... | |||||||||||||
Medical condition: Pediculosis capitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000839-33 | Sponsor Protocol Number: LP0053-1108 | Start Date*: 2016-03-23 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Safety and Effect of LEO 90100 aerosol foam on the HPA Axis and Calcium Metabolism in Adolescent Subjects (Aged 12 to < 17 Years) with Plaque Psoriasis A phase 2 trial evaluating the safety and e... | |||||||||||||
Medical condition: Plague Psoriasis | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000380-27 | Sponsor Protocol Number: 192024-058Amendment3 | Start Date*: 2011-06-21 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Parallel-group Study to Evaluate the Safety and Efficacy of Bimatoprost Solution 0.03%, 0.1%, and 0.3% Compared with Vehicle in Women with Female Pattern Ha... | |||||||||||||
Medical condition: Female pattern hair loss | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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