- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (25)
37 result(s) found for: Onychomycosis.
Displaying page 1 of 2.
EudraCT Number: 2022-003913-12 | Sponsor Protocol Number: 22/589-EC_M. | Start Date*: 2023-03-07 |
Sponsor Name:COMPLUTENSE UNIVERSITY OF MADRID | ||
Full Title: Diode laser and photodynamic therapy Versus Ciclopirox Hydroxypropyl Chitosan. Randomised controlled clinical trial. | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003416-31 | Sponsor Protocol Number: FAEDV-2012-01 | Start Date*: 2013-02-22 |
Sponsor Name:Fundación Academia Española de Dermatología y Venereología | ||
Full Title: Multicenter, randomized, open clinical trial comparing three sessions of methyl-aminolevulinate 16% (Metvix®) photodynamic therapy versus a group without photodynamic therapy to treat onychomycosis. | ||
Medical condition: onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004611-30 | Sponsor Protocol Number: BT0400-208-BEL | Start Date*: 2006-02-14 |
Sponsor Name:Barrier Therapeutics nv | ||
Full Title: An open label phase IIa trial to assess efficacy and tolerability of a once a week oral dose of 200 mg R126638 in disto-lateral toenail onychomycosis. | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000561-31 | Sponsor Protocol Number: PM1331 | Start Date*: 2015-06-15 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL, VEHICLE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF P-3058 10% NAIL SOLUTION IN THE TREATMENT OF ONYCHOMYCOSIS | |||||||||||||
Medical condition: Mild to moderate distal subungual Onychomycosis caused by Dermatophytes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) BG (Completed) SE (Completed) DE (Completed) SK (Completed) BE (Completed) PL (Completed) CZ (Completed) LT (Completed) GR (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001028-11 | Sponsor Protocol Number: K70-2 | Start Date*: 2007-05-24 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A double-blind, placebo-controlled study of efficacy, safety and tolerability of topical Kaprolac® K70 in six months treatment of distal subungual onychomycosis (DSO) | |||||||||||||
Medical condition: Distal subungual onychomycosis (DSO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000544-26 | Sponsor Protocol Number: RD.03.SPR.29106 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Determination of antifungal activity of Loceryl® Nail Lacquer 5% when used concomitantly with a cosmetic nail varnish compared to a Loceryl® Nail Lacquer 5% alone in treatment of toenail Distal Sub... | |||||||||||||
Medical condition: Mild to moderate toenail Distal Subungual Onychomycosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011125-14 | Sponsor Protocol Number: RV4104A-2008-548 | Start Date*: 2009-07-06 | |||||||||||
Sponsor Name:Pierre Fabre Dermatologie | |||||||||||||
Full Title: A multicentre, randomized, controlled study of the efficacy, safety and cost-effectiveness of a sequential therapy with RV4104A ointment, ciclopiroxolamine cream and ciclopirox film-forming solutio... | |||||||||||||
Medical condition: Patients suffering from distal-lateral or lateral subungual onychomycosis of one great toenail (the target nail) without matrix involvement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005595-17 | Sponsor Protocol Number: PMPed-004 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: Multicentre, open label study to assess the tolerability of P-3058 nail solution in paediatric patients affected by mild-to-moderate onychomycosis | |||||||||||||
Medical condition: Onychomycosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) BE (Completed) LV (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005905-51 | Sponsor Protocol Number: W0003-01 | Start Date*: 2006-02-20 |
Sponsor Name:Stiefel Laboratories (Maidenhead) Limited trading as Stiefel International Research and Development | ||
Full Title: A PHASE II, SINGLE CENTRE, RANDOMISED, PARALLEL GROUP, CLINICAL STUDY TO INVESTIGATE THE TOLERABILITY OF DOUBLE BLIND CICLOPIROX NAIL PRODUCT COMPARED TO DOUBLE BLIND PLACEBO NAIL PRODUCT COMPARED ... | ||
Medical condition: Mild to moderate onychomycosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003508-21 | Sponsor Protocol Number: CSFO327N2302 | Start Date*: 2006-10-20 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, vehicle-controlled, multicenter, parallel group study to assess the efficacy, safety, and tolerability of topical terbinafine hydrogen chloride (HCl) formulation for 24 ... | |||||||||||||
Medical condition: Onychomycosis (mild to moderate) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006338-17 | Sponsor Protocol Number: CL-067-II-01 | Start Date*: 2007-08-22 | |||||||||||
Sponsor Name:CPDS BERMUDA, LTD. | |||||||||||||
Full Title: OPEN-LABEL STUDY OF EFFICACY AND SAFETY OF 067 (TERBINAFINE IN TRANSFERSOME®) FOR THE TREATMENT OF ONYCHOMYCOSIS | |||||||||||||
Medical condition: Bilateral onychomycosis of the hallux nail (great toe) with positive mycosis culture and KOH microscopy as per central laboratory, otherwise healthy according to physical examination | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003570-10 | Sponsor Protocol Number: CSFO327N2303 | Start Date*: 2007-03-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open-label, active-controlled, multicenter, parallel group study to assess the efficacy, safety and tolerability of topical 10% terbinafine hydrogen chloride (HCl) formulation versus ... | |||||||||||||
Medical condition: mild to moderate toenail onychomycosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) FI (Completed) HU (Completed) ES (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001503-31 | Sponsor Protocol Number: RD.03.SPR.105078 | Start Date*: 2015-11-30 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject adherence and satisfaction for treatment of Onychomycosis with Loceryl® Nail Lacquer 5% versus Canesten® Fungal Nail Treatment Set | |||||||||||||
Medical condition: Mycological confirmed toenail Distal and Lateral Subungual Onychomycosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002418-23 | Sponsor Protocol Number: W0027-10 | Start Date*: 2008-12-17 | ||||||||||||||||
Sponsor Name:Stiefel Laboratories Inc. | ||||||||||||||||||
Full Title: A phase 2, randomized, double-blind, placebo-controlled, parallel-group, dose-ranging study to investigate the efficacy and safety of 4 dose regimens of oral albaconazole in subjects with distal su... | ||||||||||||||||||
Medical condition: Distal subungual onychomycosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IS (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000974-54 | Sponsor Protocol Number: RD.03.SPR.40026 | Start Date*: 2007-02-28 | |||||||||||
Sponsor Name:GALDERMA Research & Development | |||||||||||||
Full Title: A multi-centre, randomized, parallel groups, vehicle and active controlled study of amorolfine 4% and 10% nail lacquer new formulation in the topical treatment of distal and lateral subungual toena... | |||||||||||||
Medical condition: Distal and lateral subungual onychomycosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005895-42 | Sponsor Protocol Number: TLT-CLI-001 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:TLT Medical Ltd. | |||||||||||||
Full Title: A study to determine the safety and efficacy of a terbinafine topical formulation system in subjects with onychomycosis in laser treated toenails versus ciclopirox lacquer in intact toenails | |||||||||||||
Medical condition: Distal/lateral Subungual onychomycosis (DSO) caused by dermatophytes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013261-26 | Sponsor Protocol Number: K101-I | Start Date*: 2009-08-19 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A double-blind, randomized, multi-centre, placebo-controlled study of efficacy and safety of topical K101 in twelve months treatment of distal subungual onychomycosis (DSO) | |||||||||||||
Medical condition: Distal subungual onychomycosis (DSO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003506-25 | Sponsor Protocol Number: CSFO327N2301 | Start Date*: 2007-03-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, vehicle-controlled, multicenter, parallel group study to assess the efficacy, safety, and tolerability of topical terbinafine hydrogen chloride (HCl) formulation for 24 ... | |||||||||||||
Medical condition: Onychomycosis (mild to moderate) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001237-24 | Sponsor Protocol Number: RD.03.SPR.105082 | Start Date*: 2015-07-28 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject adherence and satisfaction for treatment of Onychomycosis with Loceryl® Nail Lacquer 5% versus Ciclopoli® Nail Lacquer. | |||||||||||||
Medical condition: Toenail Distal and Lateral Subungual Onychomycosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002707-10 | Sponsor Protocol Number: PM0731 | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Polichem SA | |||||||||||||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE BLIND WITHIN FREQUENCY OF ADMINISTRATION, PLACEBO CONTROLLED, DOSE-FINDING, PARALLEL-GROUP, EFFICACY AND SAFETY STUDY OF 3 DOSES OF P-3058 NAIL LACQUER (5% o.d., 10%... | |||||||||||||
Medical condition: Mild to moderate distal subungual Onychomycosis due to Dermatophytes. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) LV (Completed) IT (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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