- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (31)
15 result(s) found for: Tinea pedis.
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EudraCT Number: 2008-002399-92 | Sponsor Protocol Number: MP/clin/001-Ter | Start Date*: 2008-10-08 | |||||||||||
Sponsor Name:MedPharm Ltd. | |||||||||||||
Full Title: A phase IIa randomised, observer-blind, comparative study of the efficacy, tolerability and consumer acceptability of topical MedSpray™ TP 1 % versus Lamisil® Once 1 % in the treatment of tinea pedis | |||||||||||||
Medical condition: tinea pedis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002851-40 | Sponsor Protocol Number: CLOTAIS01/2019 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:ANTIBIOTICE SA | |||||||||||||
Full Title: A Randomized, Parallel Design, Multiple-Site Study to Evaluate the non-inferiority of generic Clotrimazole 10mg/g cream (Antibiotice SA) compared to Canesten® 10mg/g cream in Patients with Tinea Pedis | |||||||||||||
Medical condition: Tinea Pedis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Trial now transitioned) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016626-14 | Sponsor Protocol Number: H552000-0919 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: A Phase IIa, two-center, randomized, double-blind study with parallel groups to evaluate the anti-mycotic and anti-inflammatory efficacy of topical combinational product LAS 41003 versus correspond... | |||||||||||||
Medical condition: 120 male or female patients with symptomatic moderate to severe tinea pedis will be randomized | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004695-49 | Sponsor Protocol Number: 08-01 / Ter-C | Start Date*: 2009-01-13 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Doppelblinde, randomisierte klinische Studie zum Vergleich der Wirksamkeit und Verträglichkeit von Terbinafin Creme 1% vs. Lamisil® Creme vs. Grundlage bei Patienten mit Tinea pedis | |||||||||||||
Medical condition: Tinea pedis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005654-21 | Sponsor Protocol Number: 13957 | Start Date*: 2009-09-11 | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: An investigator-blind, randomized, multicenter, 5-arm, placebo- and active controlled parallel group pilot trial to explore the efficacy and tolerability of topical bifonazole liquid spray in patie... | |||||||||||||
Medical condition: Athlete’s foot, moderate severity. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000775-15 | Sponsor Protocol Number: TERBI 06/05 | Start Date*: 2006-09-11 |
Sponsor Name:PLIVA - ISTRAŽIVANJE I RAZVOJ d.o.o. | ||
Full Title: Double blind, comparative, randomized, placebo controlled, clinical study of therapeutic equivalence and tolerability of the topical preparation Terbinafine cream 1% (Pliva Croatia) with the medica... | ||
Medical condition: Uncomplicated Tinea pedis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007067-16 | Sponsor Protocol Number: TERJ001 | Start Date*: 2009-02-11 |
Sponsor Name:JELFA SA | ||
Full Title: Randomised, double-blind, parallel-group, comparative study of two terbinafine products | ||
Medical condition: tinea pedis (interdigital, Athlet´s foot) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002644-23 | Sponsor Protocol Number: MB_PDT_1 | Start Date*: 2020-07-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Dept. of Dermatology, Zealand University Hospital, Roskilde | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Photodynamic therapy of antifungal resistant dermatophytes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Competent patients over 18 years old with mycological verified antifungal resistant dermatophytosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006513-33 | Sponsor Protocol Number: KETFUN3001 | Start Date*: 2007-05-23 |
Sponsor Name:Janssen Pharmaceutica NV | ||
Full Title: A double-blind, randomized, parallel group comparison of Nizoral® cream (F012), ketoconazole 2% cream (F126) and placebo (F000) in the treatment of interdigital Tinea Pedis. | ||
Medical condition: For the treatment of tinea pedis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001263-32 | Sponsor Protocol Number: 241011BS | Start Date*: 2006-07-21 |
Sponsor Name:York Pharma GmbH | ||
Full Title: Phase III study to evaluate the anti-mycotic efficacy of a topical Abafungin formulation in patients with tinea pedis | ||
Medical condition: Patients with tinea pedis interdigitalis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000940-10 | Sponsor Protocol Number: RE&D VÚFB/8/2005/Tol-5 | Start Date*: 2005-07-04 |
Sponsor Name:RE&D VÚFB, s.r.o. | ||
Full Title: Evaluation of tolerance and efficacy of preparation TERBINAFIN HBF CREAM (Herbacos-Bofarma) and its comparison with preparation LAMISIL CREAM (Novartis) in patients with interdigital form of tinea ... | ||
Medical condition: tinea pedis var. interdigitale | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002112-26 | Sponsor Protocol Number: 139B7 | Start Date*: 2007-05-21 |
Sponsor Name:YORK Pharma GmbH | ||
Full Title: Open, single-arm phase-III study to investigate the percutaneous absorption of abafungin after topical dermal application of Abafungin cream 1.0 % (YORK Pharma GmbH) in 20 patients with tinea pedis... | ||
Medical condition: Tinea pedis interdigital | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002842-20 | Sponsor Protocol Number: 241012BS | Start Date*: 2005-09-29 |
Sponsor Name:York Pharma GmbH | ||
Full Title: Phase II dose ranging study to evaluate the anti-mycotic efficacy of topical Abafungin formulations in patients with tinea pedis. | ||
Medical condition: patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001242-25 | Sponsor Protocol Number: BBT120126032001 | Start Date*: 2017-02-07 | ||||||||||||||||
Sponsor Name:Blueberry Therapeutics Ltd. | ||||||||||||||||||
Full Title: An Early Phase Development, Partly Blinded, Positive and Vehicle Controlled, Randomized, Non-inferiority Investigation of the Pharmacokinetics, Safety and Efficacy of BB2603 Cutaneous Hand-Pump Spr... | ||||||||||||||||||
Medical condition: Onychomycosis and associated Tinea Pedis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001239-32 | Sponsor Protocol Number: EBERTOIII/05ES01 | Start Date*: 2005-09-02 | |||||||||||
Sponsor Name:Laboratorios SALVAT, S.A. | |||||||||||||
Full Title: Ensayo clínico multicéntrico, aleatorizado, paralelo, doble ciego, para evaluar la eficacia y seguridad de eberconazol solución 1% frente a placebo en el tratamiento de las dermatofitosis | |||||||||||||
Medical condition: Dermatofitosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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