- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (16)
26 result(s) found for: Shampoo.
Displaying page 1 of 2.
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: 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: 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: 2007-007315-93 | Sponsor Protocol Number: V00071 GM 101 1A | Start Date*: 2008-03-25 |
Sponsor Name:Pierre Fabre dermatologie | ||
Full Title: Human skin blanching essay comparing a new shampoo containing betamethasone dipropionate at 0.025% and 0.050% to three reference marketed formulations in healthy subjects | ||
Medical condition: As it's a Mc Kensie and Stoughton test, there is no medical condition to be investigated in this trial. The intended indication for the betamethasone dipropionate shampoo is seborrhoeic dermatitis ... | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005795-13 | Sponsor Protocol Number: Ketoil 01/07 | Start Date*: 2007-11-12 | |||||||||||
Sponsor Name:MIPHARM | |||||||||||||
Full Title: EFFICACY AND SAFETY ASSESSMENT OF KETOIL, SHAMPOO CONTAINING KETOCONAZOLE 0.5% SERENOA REPENS (SAW PALM) AND TAURINE, IN THE TREATMENT OF PATIENTS AFFECTED BY DANDRUFF AND SEBORRHEIC DERMATITIS COM... | |||||||||||||
Medical condition: dandruff and seborroic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
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: 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: 2014-004666-14 | Sponsor Protocol Number: LACAC_L_04678 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Safety Dermatological Evaluation: acceptability with pediatric follow up – Dermacyd Infantile LACAC_L_04678 | |||||||||||||
Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013276-46 | Sponsor Protocol Number: N/A | Start Date*: 2010-02-05 |
Sponsor Name:Queen Victoria Hospital | ||
Full Title: The effect of oral Ivermectin on Demodex associated blepharitis | ||
Medical condition: Demodex Follicularum associated anterior blepharitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020206-14 | Sponsor Protocol Number: 09.0058 | Start Date*: 2011-01-31 |
Sponsor Name:St George's University of London | ||
Full Title: Evaluation study of Meticillin Resistant Staphylococcus aureus (MRSA) during routine nasal decolonisation programmes with Bactroban Nasal® ointment, Chlorhexidine Gluconate 4% body and hair wash, a... | ||
Medical condition: MRSA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000613-22 | Sponsor Protocol Number: CO-150225133959-HRCT | Start Date*: 2018-10-15 |
Sponsor Name:Johnson & Johnson Consumer Inc | ||
Full Title: A 16 Week, Single-center, Randomized, Placebo- and Active-controlled Proof of Principle Study to Assess the Efficacy and Safety of a 5% Minoxidil Topical Gel Formulation in Male subjects with Andro... | ||
Medical condition: Alopecia Androgentica | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2023-000463-32 | Sponsor Protocol Number: CB-03-01/25 | Start Date*: 2023-04-19 | |||||||||||
Sponsor Name:CASSIOPEA SpA | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) Cream, 1% Applied Twice Daily for 12 Weeks in... | |||||||||||||
Medical condition: Facial Acne Vulgaris | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000461-13 | Sponsor Protocol Number: 171-7151-201 | Start Date*: 2023-04-19 |
Sponsor Name:Intrepid Therapeutics Inc. | ||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Vehicle-Controlled, Dose Escalating Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) Cream Applied Once or Twice-... | ||
Medical condition: Facial Acne Vulgaris | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-002637-21 | Sponsor Protocol Number: CB-03-01/27 | Start Date*: 2016-06-24 | |||||||||||
Sponsor Name:CASSIOPEA SpA | |||||||||||||
Full Title: An Open-Label, Long-Term Extension Study to Evaluate the Safety of Cortexolone 17α-Propionate (CB-03-01) Cream, 1% Applied Twice-Daily in Subjects with Acne Vulgaris | |||||||||||||
Medical condition: Facial and truncal acne vulgaris | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002623-26 | Sponsor Protocol Number: CB-03-01/26 | Start Date*: 2016-03-17 | |||||||||||
Sponsor Name:CASSIOPEA SpA | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) 1% Cream Applied Twice-Daily for 12 Weeks in ... | |||||||||||||
Medical condition: facial acne vulgaris | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004998-83 | Sponsor Protocol Number: MUS92579_2057_1 | Start Date*: 2012-04-04 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: A Double-Blind, Randomized, Dose Selection Vehicle–Controlled Multicenter Clinical Study for Evaluation of the Safety, Tolerability, Efficacy, and Pharmacokinetics of topical Neramexane in Subjects... | |||||||||||||
Medical condition: Moderate to severe acne | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021193-11 | Sponsor Protocol Number: HT-07 | Start Date*: 2010-09-14 | |||||||||||
Sponsor Name:Helperby Thearapeutics Ltd | |||||||||||||
Full Title: A randomised, open-labelled, multiple dose study of HT61 formulations applied to the anterior nares plus chlorhexidine body and hair washes in subjects with nasal carriage of Staphylococcus aureus | |||||||||||||
Medical condition: Nasal carriage of Staphylococcus aureus (including MRSA) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2009-017398-39 | Sponsor Protocol Number: HT-04 | Start Date*: 2010-02-02 | |||||||||||
Sponsor Name:Helperby Thearapeutics Ltd | |||||||||||||
Full Title: Randomised double-blind, vehicle controlled dosing frequency study of HT61 1% gel applied to the anterior nares plus chlorhexidine body and hair washes in subjects with nasal carriage of Staphyloco... | |||||||||||||
Medical condition: Nasal carriage of Staphylococcus aures (including MRSA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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