- Trials with a EudraCT protocol (1,106)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,106 result(s) found for: Skin and Connective Tissue Diseases.
Displaying page 24 of 56.
EudraCT Number: 2013-004158-81 | Sponsor Protocol Number: 200398 | Start Date*: 2017-09-21 | |||||||||||
Sponsor Name:GlaxoSmithKline GmbH & Co. KG | |||||||||||||
Full Title: A multi-centre, single-blind, parallel group, clinical evaluation of the efficacy and safety of clindamycin 1% / benzoyl peroxide 3% and azelaic acid 20% in the topical treatment of mild to moder... | |||||||||||||
Medical condition: Acne Vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003845-40 | Sponsor Protocol Number: 122-0551-209 | Start Date*: 2019-07-09 | |||||||||||
Sponsor Name:Mayne Pharma LLC | |||||||||||||
Full Title: An open label evaluation of the adrenal suppression potential and pharmacokinetic properties of twice daily halobetasol propionate foam, 0.05% in subjects 12 to less than 18 years of age with plaqu... | |||||||||||||
Medical condition: Plaque psoriasis | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006308-12 | Sponsor Protocol Number: TSP-RAP-1 | Start Date*: 2012-07-16 |
Sponsor Name:Fundación Investigación Hospital Ramón y Cajal | ||
Full Title: phase II clinical trial, to study the efficacy and safety of topical rapamycin in reducing facial angiofibromas. | ||
Medical condition: Facial tumors (angiofibromas) associated with tuberous sclerosis complex. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000478-32 | Sponsor Protocol Number: B?PRPtendon2013 | Start Date*: 2013-07-12 | |||||||||||
Sponsor Name:Jose Ignacio Martin Gomez | |||||||||||||
Full Title: Pilot randomised trial to assess the safety and potential efficacy of platelet rich plasma tenotomy for the treatment of chronic epicondylitis | |||||||||||||
Medical condition: epicondylitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000063-16 | Sponsor Protocol Number: RD.03.SPR.109807 | Start Date*: 2016-06-10 | |||||||||||
Sponsor Name:Galderma R&D SNC | |||||||||||||
Full Title: Efficacy and safety of CD5024 1% in acne vulgaris | |||||||||||||
Medical condition: Acne vulgaris | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002266-40 | Sponsor Protocol Number: CAIN457ADE02 | Start Date*: 2013-12-09 |
Sponsor Name:Novartis Pharma GmbH | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, exploratory evaluation of surrogate markers of cardiovascular risk in patients with active chronic plaque-type psoriasis treated for 52 ... | ||
Medical condition: active chronic plaque-type psoriasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004612-10 | Sponsor Protocol Number: BAY86-5300/91772 | Start Date*: 2015-01-12 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A multicenter, double-blind, randomized, placebo controlled study to evaluate the efficacy and safety of an oral contraceptive preparation YAZ (drospirenone 3 mg / ethinylestradiol 20 µg) for 6 tre... | |||||||||||||
Medical condition: Acne Vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006283-42 | Sponsor Protocol Number: KAD166 | Start Date*: 2012-04-30 | |||||||||||
Sponsor Name:Dr. Kade Pharmazeutische Fabrik GmbH | |||||||||||||
Full Title: Placebo-controlled double-blind trial investigating the efficacy and tolerability of Posterisan® akut with lidocaine (50 mg/g rectal ointment) in abatement of complaints associated with the anorect... | |||||||||||||
Medical condition: Relief of complaints associated with anorectal symptom complex (pain, burning, itching) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002714-45 | Sponsor Protocol Number: FJD-MET-2016-01 | Start Date*: 2017-01-13 |
Sponsor Name:Instituto de Investigación Sanitaria Fundación Jiménez Díaz | ||
Full Title: "Pilot study to assess the efficacy of treatment with metformin in patients with Hidradenitis suppurativa refractory to standard treatment " | ||
Medical condition: Hidradenitis suppurativa | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003867-21 | Sponsor Protocol Number: LP0160-1327 | Start Date*: 2017-10-30 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A phase 4 trial comparing the efficacy of subcutaneous injections of brodalumab to oral administrations of fumaric acid esters in adults with moderate to severe plaque psoriasis | |||||||||||||
Medical condition: moderate to severe plaque psoriasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 2011-004370-28 | Sponsor Protocol Number: 11-03/FusBet-C | Start Date*: 2012-06-25 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomized clinical trial to compare the efficacy and safety of fusidic acid 2% betamethasone 0,1% cream vs. Fucicort cream vs. vehicle for patients with bacterial infected eczemas. | |||||||||||||
Medical condition: Bacterial infected eczemas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005003-14 | Sponsor Protocol Number: Pro_MC2-01_13_Biotek | Start Date*: 2014-04-02 |
Sponsor Name:Drug Delivery Solutions ApS | ||
Full Title: A randomized, multi-centre, observer-blind, controlled exploratory study to assess efficacy and safety of new topical formulations (MC2-01) in patients with plaque psoriasis | ||
Medical condition: Patients with stable plaque type psoriasis (sufficient number and size of psoriatic plaques(s) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001442-35 | Sponsor Protocol Number: PTZ | Start Date*: 2021-06-04 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: A PHASE 2 MONOCENTRIC PILOT STUDY TO EVALUATE THE EFFICACY AND SAFETY PROFILE OF PIOGLITAZONE IN SUBJECTS WITH ACTIVE NON-SEGMENTAL VITILIGO | |||||||||||||
Medical condition: NON SEGMENTAL VITILIGO WITH BSA BETWEEN 2% AND 50% AND A NON-SATISFACTORY RESPONSE (LESS THAN 10%) TO A PREVIOUS PHOTOTHERAPY CYCLE | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000294-78 | Sponsor Protocol Number: CTP001H | Start Date*: 2019-06-07 |
Sponsor Name:Nektr Technologies | ||
Full Title: A Randomized, Single-Blinded, Comparative Study of Mycosinate and Curanail in the Treatment of Fungal Nail Infection | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-000097-30 | Sponsor Protocol Number: 2018-PSO-IL17R | Start Date*: 2018-04-18 | |||||||||||
Sponsor Name:Herlev and Gentofte Hospital | |||||||||||||
Full Title: Efficacy of brodalumab in patients with psoriasis with failure of other anti-IL-17 treatments | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001971-38 | Sponsor Protocol Number: HARRAS1/2006 | Start Date*: 2012-01-05 |
Sponsor Name:HARRAS-PHARMA-CURARINA GmbH | ||
Full Title: Comparative Study with a Propolis Cream vs. Aciclovir Cream in Patients with Herpes labialis A single-blind, randomised, two-arm study | ||
Medical condition: Herpes labialis Single-blind, randomised, controlled parallel group comparison of a Propolis special extract GH 2002 cream (Herpetino® Balsam) and an aciclovir 5% containing cream. Up to 10 day... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004372-19 | Sponsor Protocol Number: HARRAS1/2012 | Start Date*: 2013-06-05 |
Sponsor Name:HARRAS-PHARMA-CURARINA GmbH | ||
Full Title: Comparative Study with a Propolis Cream vs. Aciclovir Cream in Patients with Herpes labialis A double-blind, randomised, two-arm study | ||
Medical condition: Herpes labialis Double-blind, randomised, controlled parallel group comparison of a Propolis special extract GH 2002 cream (Herpetino® Balsam) and an aciclovir 5% containing cream. Up to 10 day... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000334-30 | Sponsor Protocol Number: INT27/14 | Start Date*: 2014-09-17 | |||||||||||
Sponsor Name:Fondazione IRCCS ''IStituto Nazionale dei Tumori'' | |||||||||||||
Full Title: Immunomodulatory effect of esomeprazole antitumoral and high-dose under neoadjuvant and adjuvant in patients with melanoma in stage III. Randomized pilot study treatment vs control | |||||||||||||
Medical condition: metastatic melanoma BLS+ and BRAF wt | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003691-23 | Sponsor Protocol Number: 50621 | Start Date*: 2014-11-10 |
Sponsor Name:Maastricht Universitair Medisch Centrum | ||
Full Title: Topical Ingenol mebutate versus 5% 5-fluorouracil versus 5% Imiquimod versus photodynamic therapy in the treatment of actinic keratosis: a multi-center randomized efficacy and cost-effectiveness st... | ||
Medical condition: Actinic keratosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
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