- Trials with a EudraCT protocol (3,724)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (646)
3,724 result(s) found for: Skin.
Displaying page 1 of 187.
EudraCT Number: 2004-002398-22 | Sponsor Protocol Number: CL-070-II-01 | Start Date*: 2005-01-27 | |||||||||||
Sponsor Name:IDEA AG | |||||||||||||
Full Title: Double-blind, placebo-controlled study to investigate the efficacy and safety of IDEA-070 (ketoprofen in Transfersome®) in different dermatological diseases | |||||||||||||
Medical condition: Patients with different dermatological diseases Atopic eczema (MedDRA 6.0, LLT: 10003641) Dishydrotic hand eczema (MedDRA 6.0, LLT: 10013913) Plaque type psoriasis (MedDRA 6.0, LLT: 10050576)... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002995-17 | Sponsor Protocol Number: 35820 | Start Date*: 2011-08-15 |
Sponsor Name: | ||
Full Title: Treatment trial of stiff skin syndrome with Losartan | ||
Medical condition: Stiff skin syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002175-28 | Sponsor Protocol Number: DACOMINT14 | Start Date*: 2014-08-04 | |||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | |||||||||||||
Full Title: Efficacy and safety of single agent pan-HER inhibitor Dacomitinib in the treatment of locally advanced unresectable or metastatic squamous cell cancer of the skin or with clinical contraindication... | |||||||||||||
Medical condition: locally advanced unresectable or metastatic squamous cell cancer of the skin or with clinical contraindication to surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011455-51 | Sponsor Protocol Number: AA0906 | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Department of Oncology, University Hospital Herlev | |||||||||||||
Full Title: Palliative treatment of ulcerated cutaneous metastases: Randomised trial between electrochemotherapy and radiotherapy | |||||||||||||
Medical condition: Ulcerated cutaneous metastases from solid tumor cancers is a particularly difficult problem with painful skin ulceration, maladorous discharge and bleeding. The intention of this study is to invest... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003495-31 | Sponsor Protocol Number: CCLL442X2201 | Start Date*: 2017-12-14 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, Investigator-and patient-blind, placebo-controlled, parallel group first in human and proof of concept study to evaluate the safety, tolerability, and efficacy of CLL442 in patients w... | |||||||||||||
Medical condition: Cutaneous Squamous Cell Carcinoma in situ (SCCis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005626-29 | Sponsor Protocol Number: TR02ext | Start Date*: 2015-01-21 | |||||||||||
Sponsor Name:Trevi Therapeutics, Inc. | |||||||||||||
Full Title: An Open Label Extension Study of the Safety and Anti-Pruritic Efficacy of Nalbuphine HCL ER Tablets in Hemodialysis Patients with Uremic Pruritus | |||||||||||||
Medical condition: Uremic Pruritis in Hemodialysis Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004113-13 | Sponsor Protocol Number: M602011070 | Start Date*: 2020-08-17 | |||||||||||||||||||||||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||||||||||||||||||||||
Full Title: A prospective, randomized, double-blind, placebo-controlled, multicenter study with an open-label extension period to investigate the efficacy and safety of NT 201 in the simultaneous treatment of ... | |||||||||||||||||||||||||||||||||
Medical condition: Moderate to severe upper facial lines (horizontal forehead lines, glabellar frown lines, and lateral canthal lines) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017241-55 | Sponsor Protocol Number: RC 43/08 | Start Date*: 2009-12-09 | |||||||||||
Sponsor Name:ISTITUTO PER L`INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Open randomized study on propranolol vs prednisone for haemangioma in patients younger than 18 months of age | |||||||||||||
Medical condition: Haemagiomas | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022440-20 | Sponsor Protocol Number: 10-PP-11 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Traitements of angioma plans of the child by laser to pulsed colouring agent and Timolol (Néogel 0,1%). | |||||||||||||
Medical condition: Angioma plans | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001936-11 | Sponsor Protocol Number: 3074K4-3339-WW | Start Date*: 2009-03-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind Study to Evaluate the Safety and Efficacy of Tigecycline Versus Clindamycin for the Treatment of Complicated Skin and Skin Structure Infections, Inc... | |||||||||||||||||||||||||||||||||
Medical condition: Complicated skin and skin structure infection (cSSSI) with or without methicillin-resistant Staphylococcus aureus (MRSA) | |||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013455-30 | Sponsor Protocol Number: AOBS-ECT-CH | Start Date*: 2009-12-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: EFFICACY OF ELETTROPORATION COMBINED WITH BLEOMYCIN IN THE TREATMENT OF KELOIDS AND HYPERTROPHIC SCARS: A PILOT STUDY | |||||||||||||
Medical condition: KELOIDS AND HYPERTROPHIC SCARS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000314-15 | Sponsor Protocol Number: LPS15991 | Start Date*: 2021-08-17 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: Open label exploratory study to evaluate the effect of dupilumab on skin barrier function in patients with moderate to severe atopic dermatitis | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001518-40 | Sponsor Protocol Number: LPS16764 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:Sanofi Aventis Recherche & Developpement | |||||||||||||
Full Title: Open-label exploratory study to evaluate the effect of dupilumab on skin barrier function in pediatric patients with moderate to severe atopic dermatitis | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003765-10 | Sponsor Protocol Number: I-Tackle | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Immunotherapy Followed By EGFR Inhibitor In Locally Advanced Or Metastatic Squamous Cell Cancer Of The Skin: Tackling Primary And Secondary Resistance | |||||||||||||
Medical condition: Patient with Locally Advanced Or Metastatic Squamous Cell Cancer Of The Skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001753-26 | Sponsor Protocol Number: DC0984LE401 | Start Date*: 2013-07-25 | ||||||||||||||||||||||||||
Sponsor Name:Pierre Fabre Dermo-cosmétique | ||||||||||||||||||||||||||||
Full Title: Clinical and biophysics evaluation of the cutaneous modifications following the local use of a lotion containing 0,1 % of trétinoïne. | ||||||||||||||||||||||||||||
Medical condition: Acne | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001318-39 | Sponsor Protocol Number: UNIHHSkinQuality202000401 | Start Date*: 2021-04-30 |
Sponsor Name:Prof. Dr. Martina Kerscher, University of Hamburg | ||
Full Title: Skin perception after intradermal application of IncobotulinumtoxinA within upper and midface (Interventional Phase II) | ||
Medical condition: Skin perception after intradermal application of INCOBOTULINUMTOXIN A within upper and midface | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001774-88 | Sponsor Protocol Number: TAR-ORI-SD001 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Targanta Therapeutics Corporation | |||||||||||||
Full Title: Nuvocid™ (oritavancin) at Single or Infrequent Doses for the Treatment of Complicated Skin and Skin Structure Infections (SIMPLIFI) | |||||||||||||
Medical condition: Complicated skin and skin structure infections (cSSSI). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006863-35 | Sponsor Protocol Number: 314759 | Start Date*: 2013-10-01 | |||||||||||||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||||||||||||
Full Title: Prophylactic photodynamic therapy for organ transplant patients – a randomised, intra-individual trial with blinded outcome evaluation. | |||||||||||||||||||||||
Medical condition: Development of actinic keratoses and skin cancer in kidney transplant patients - a randomised, intra-individual trial with blinded outcome evaluation. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006272-11 | Sponsor Protocol Number: JWGZDVDT0107 | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:J.W. Goethe University Hospital | |||||||||||||
Full Title: Validation of Dermatophot for the assessment of steroid induced skin atrophy | |||||||||||||
Medical condition: To investigate and establish a new simple method Dermatophot® score for the evaluation of skin atrophy (damage) after the usage of moderate-potent or super-potent topical steroids. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000427-17 | Sponsor Protocol Number: CY503C1 | Start Date*: 2007-10-26 | |||||||||||
Sponsor Name:CYTAVIS BioPharma GmbH | |||||||||||||
Full Title: A phase II multicenter study to test progression- free and overall survival of CY-503 in the treatment of patients with unresectable stage IV metastatic melanoma after antineoplastic treatment failure | |||||||||||||
Medical condition: unresectable progressive metastatic melanoma stage IV after antineoplastic treatmet failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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