- Trials with a EudraCT protocol (446)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
446 result(s) found for: Barrier cream.
Displaying page 1 of 23.
EudraCT Number: 2004-004824-11 | Sponsor Protocol Number: ELBE-2005 | Start Date*: 2005-04-15 |
Sponsor Name:Universitätshautklinik Kiel | ||
Full Title: Role for pimecrolimus in restoring skin barrier function and normalizing epidermal lipid content and differentiation in atopic epidermis: a randomized, intra-patient, double-blind (right/left arm) ... | ||
Medical condition: Atopic Dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-006208-21 | Sponsor Protocol Number: ELKE-2006 | Start Date*: 2006-10-23 |
Sponsor Name:Department of Dermatology, University of Kiel | ||
Full Title: Clinical Efficacy of Pimecrolimus Cream in Seborrheic Dermatitis. Efficacy of pimecrolimus in normalizing clinical symptoms, explorative study of barrier function, hydration, lipid content and diff... | ||
Medical condition: Efficacy of pimecrolimus in normalizing clinical symptoms, explorative study of barrier function, hydration, lipid content and differentiation in seborrheic dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001469-42 | Sponsor Protocol Number: 35328 | Start Date*: 2011-06-27 |
Sponsor Name:Deventer Ziekenhuis | ||
Full Title: A randomised clinical trial on the effectiveness of MediHoney barrier cream versus the standard therapy with zinc oxide in the treatment of intertrigo. | ||
Medical condition: intertrigo | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003106-99 | Sponsor Protocol Number: ELBE II-2007 | Start Date*: 2007-10-04 |
Sponsor Name:University of Kiel, Department of Dermatology | ||
Full Title: Pimecrolimus and Epidermal Barrier Function: Role for pimecrolimus in restoring skin barrier function and normalizing epidermal lipid content and differentiation in atopic epidermis: a randomized, ... | ||
Medical condition: Investigative study of pathogenesis/treatment of calcineurin inhibitor vs. corticosteroid confirmatory study to prior study: Pimecrolimus and Epidermal Barrier Function, Protocol No. ELBE-2005, Eud... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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: 2018-000900-40 | Sponsor Protocol Number: LP0133-1273 | Start Date*: 2019-01-15 | ||||||||||||||||
Sponsor Name:LEO Pharma A/S | ||||||||||||||||||
Full Title: A phase 2b, double-blind, randomised, 5-arm, vehicle-controlled, dose-ranging trial to evaluate the efficacy and safety of twice daily topical application of delgocitinib cream 1, 3, 8, and 20 mg/g... | ||||||||||||||||||
Medical condition: Chronic hand eczema | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2008-000552-27 | Sponsor Protocol Number: ACO2008-CT-01 | Start Date*: 2008-06-11 |
Sponsor Name:ACO HUD NORDIC AB | ||
Full Title: Effect of moisturizing creams on skin barrier function and prevention of Malassezia recurrence in patients with atopic eczema | ||
Medical condition: Dry skin barrier disorders such as atopic eczema and ichtyosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017647-34 | Sponsor Protocol Number: ANTIRESDEV | Start Date*: 2010-03-29 | |||||||||||
Sponsor Name:Helperby Therapeutics | |||||||||||||
Full Title: Effect of minocycline and amoxicillin administration on the prevalence of antibiotic resistant bacteria and on the indigenous oral, faecal, cutaneous and nasal microbiotas. | |||||||||||||
Medical condition: Amoxicillin and Minocycline are marketed antibiotic to fight bacterial infections. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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) |
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: 2019-002643-23 | Sponsor Protocol Number: STH19966 | Start Date*: 2020-03-23 | ||||||||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: Validation of a novel composite of skin biomarkers as a primary outcome measure for evaluating the safety of treatments for atopic dermatitis: a randomized controlled trial (phase 2) comparing the ... | ||||||||||||||||||
Medical condition: atopic eczema (synonym atopic dermatitis) and the adverse treatment side effect epidermal atrophy | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004316-31 | Sponsor Protocol Number: FPP4-DE-401 | Start Date*: 2009-02-23 | |||||||||||
Sponsor Name:Novartis Consumer Health S.A. | |||||||||||||
Full Title: A randomised, double-blind, vehicle controlled, single centre, parallel group, comparative study of the efficacy of penciclovir 10 mg/g (1%) cream in preventing the appearance of classical lesions ... | |||||||||||||
Medical condition: Cold Sores caused by the herpes simplex virus (HSV) type 1. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005792-15 | Sponsor Protocol Number: 250816BS | Start Date*: 2006-04-24 |
Sponsor Name:Astion Danmark A/S | ||
Full Title: Evaluation of the efficacy of topical formulations containing ASF-1075 in the prevention and treatment of contact dermatitis | ||
Medical condition: Male or female volunteers with known nickel allergy and with healthy skin in the test area, aged 18 years or older | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003608-41 | Sponsor Protocol Number: RD.06.SPR.204245 | Start Date*: 2022-01-12 | |||||||||||
Sponsor Name:Galderma S.A. | |||||||||||||
Full Title: Evaluation of acne-induced hyperpigmentation during treatment of acne vulgaris subjects with trifarotene 50 µg/g cream versus vehicle cream over 24 weeks. | |||||||||||||
Medical condition: Moderate acne vulgaris with acne-induced post-inflammatory hyperpigmentation (PIH) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003753-28 | Sponsor Protocol Number: VEN307-AF-001 | Start Date*: 2013-09-09 |
Sponsor Name:Ventrus Biosciences | ||
Full Title: A Phase 3B, Randomized, Double-Blind, Placebo-controlled, Parallel-Treatment Group, Multicenter Efficacy and Safety Study of Topical Diltiazem Hydrochloride 2% Cream in subjects with Anal Fissure | ||
Medical condition: Pain associated with anal fissures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) BG (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003739-44 | Sponsor Protocol Number: DS107E-02 | Start Date*: 2012-11-23 |
Sponsor Name:Dignity Sciences Limited | ||
Full Title: A Randomised, Double-blind, Placebo-Controlled, Phase II Study to Assess the Efficacy and Safety of Topically Applied DGLA Cream in Patients with Mild to Moderate Atopic Dermatitis | ||
Medical condition: Atopic Dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) SE (Prematurely Ended) HU (Completed) DK (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004275-11 | Sponsor Protocol Number: CASM981M2308 | Start Date*: 2005-03-25 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open-label study to investigate blood concentrations, safety, tolerability and efficacy of Elidel® Cream 1% in patients with moderate or severe seborrheic dermatitis treated topically for 3 weeks. | ||
Medical condition: Seborrheic dermatitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-002176-39 | Sponsor Protocol Number: V3002401 | Start Date*: 2022-02-07 | |||||||||||
Sponsor Name:Veru Inc. | |||||||||||||
Full Title: ARTEST - A Randomized Phase 3 Study to Evaluate the Efficacy and Safety of Enobosarm Monotherapy Versus Active Control for the Treatment of AR+/ER+/HER2- Metastatic Breast Cancer in Patients with A... | |||||||||||||
Medical condition: (AR+)/estrogen receptor positive(ER+)/human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007055-28 | Sponsor Protocol Number: P-080623-01 | Start Date*: 2009-06-04 | |||||||||||
Sponsor Name:Ferrer International, SA | |||||||||||||
Full Title: GF-001001-00 cream. A multicentre, randomised, double-blind, parallel, placebo-controlled phase II study to assess the efficacy and safety of 3 different doses of GF-001001-00 cream versus placebo... | |||||||||||||
Medical condition: Secondarily-infected traumatic lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) CZ (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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