- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Transepidermal water loss.
Displaying page 1 of 2.
| EudraCT Number: 2015-002699-26 | Sponsor Protocol Number: PREFECT | Start Date*: 2015-10-08 |
| Sponsor Name:GWT-TUD GmbH | ||
| Full Title: Pilot study of tolerability and effectivity following application of two combination topical acne products clindamycin 1% and 0.025% tretinoin gel (Acnatac® Gel), adapalen 0,1% and benzoyl peroxide... | ||
| Medical condition: acne vulgaris | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002284-14 | Sponsor Protocol Number: 1528 | Start Date*: 2012-03-14 |
| Sponsor Name:Schur Pharmazeutika GmbH & Co. KG | ||
| Full Title: Subacute local tolerance of an ointment containing 0.5% neomycin sulfate (Myacyne Salbe) | ||
| Medical condition: Sensitive skin areas under non-occlusive and occlusive conditions | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2019-002081-12 | Sponsor Protocol Number: AHV-18-A | Start Date*: 2019-12-19 |
| Sponsor Name:Amryt Research Ltd. | ||
| Full Title: An exploratory randomized, intra-individual controlled trial of the cutaneous healing properties of Petrolatum versus the vehicle for Oleogel-S10 versus no treatment when applied topically to me... | ||
| Medical condition: Not applicable, as healthy volunteers will be recruited, who will receive mechanically induced partial thickness wounds. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016571-30 | Sponsor Protocol Number: DERL-02 | Start Date*: 2010-02-01 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to determine the effects on stratum corneum of a clinical hand cleansing protocol comparing two antiseptic hand washes, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: No medical condition is to be investigated, as such. We are looking to avoid occupational hand dermatitis in healthcare professionals, simulated using a repeat hand wash cleansing protocol in heal... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| 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: 2008-000333-22 | Sponsor Protocol Number: DERL-01 | Start Date*: 2008-04-30 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to compare the effects on stratum corneum of two medical hand wash formulations, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: The study is a healthy volunteer study. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005649-12 | Sponsor Protocol Number: SUCPAT1_CTR0026 | Start Date*: 2006-12-20 |
| Sponsor Name:Regent Medical | ||
| Full Title: A 96 hour (4-application) patch test and TEWL assessment in healthy volunteers to investigate the comparative skin irritation potential of six antiseptics and two controls following cutaneous patch... | ||
| Medical condition: This trial will be carried out on healthy volunteers. Patches containing 0.2mls of each test product will be used. Each volunteer will have a single patch per product and the patches will be remov... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-005619-28 | Sponsor Protocol Number: 2012.786 | Start Date*: 2014-07-23 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Influence of lipid emulsions for parenteral nutrition on the fonctional state of cutaneous barrier | |||||||||||||
| Medical condition: patients avec une insuffisance intestinale chronique sévère recevant une nutrition parentérale au long cours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023543-15 | Sponsor Protocol Number: CL09002 | Start Date*: 2011-01-24 |
| Sponsor Name:BioCis Pharma Oy | ||
| Full Title: Double-blind, placebo-controlled, multi-centre Phase II study to investigate dose response, safety, tolerability and efficacy of topical twice daily doses of 2.5% and 5% cis-urocanic acid in compar... | ||
| Medical condition: Chronic moderate or severe atopic dermatitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-008332-90 | Sponsor Protocol Number: CL08004 | Start Date*: 2009-02-10 |
| Sponsor Name:BioCis Pharma Oy | ||
| Full Title: Double-blind, vehicle-controlled, single centre Phase I/IIa study with topical twice daily doses of 5% cis-urocanic acid to investigate pharmacokinetics, safety, tolerability, and efficacy for up t... | ||
| Medical condition: Mild to moderate plaque psoriasis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| 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: 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: 2010-018624-20 | Sponsor Protocol Number: OPM-CIC-G-H-0902 | Start Date*: 2010-05-19 |
| Sponsor Name:University Medical Center Freiburg | ||
| Full Title: Tolerance of virucidal alcohol-based hand rubs - healthy volunteer trial | ||
| Medical condition: Only healthy volunteers are included in this trial. Alcohol-based hand rubs are licensed drugs in Germany. They are indicated to perform hand disinfection by health care workers and are used within... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005075-10 | Sponsor Protocol Number: CL08002 | Start Date*: 2008-10-01 |
| Sponsor Name:BioCis Pharma Oy | ||
| Full Title: Double-blind, vehicle-controlled, two-phase, single centre Phase I/IIa study with topical twice daily doses of 5% cis-urocanic acid to investigate pharmacokinetics, safety, tolerability and efficac... | ||
| Medical condition: Chronic mild to moderate atopic dermatitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004370-96 | Sponsor Protocol Number: LG-TCS-AD | Start Date*: 2019-02-15 | |||||||||||
| Sponsor Name:Jacob Pontoppidan Thyssen | |||||||||||||
| Full Title: The effects of topical corticosteroid use on insulin sensitivity and bone turnover | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001220-35 | Sponsor Protocol Number: RC31-19-0045 | Start Date*: 2019-10-08 | |||||||||||
| Sponsor Name:CHU de Toulouse | |||||||||||||
| Full Title: A randomized double-blinded pilot study of the efficacy and safety of dupilumab versus placebo in patients with Netherton syndrome | |||||||||||||
| Medical condition: Netherton syndrome | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004278-32 | Sponsor Protocol Number: 14031972 | Start Date*: 2020-12-04 |
| Sponsor Name:Falck clinic | ||
| Full Title: Satisfaction study of split doses botulinum toxin with double frequency | ||
| Medical condition: Wrinkles, fine lines | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003210-39 | Sponsor Protocol Number: SXR001 | Start Date*: 2021-11-23 | |||||||||||
| Sponsor Name:Sixera Pharma | |||||||||||||
| Full Title: A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled, first-time-in-man (FTIM) Proof of Concept (PoC) study to evaluate the safety and efficacy of topically applie... | |||||||||||||
| Medical condition: Netherton-syndrome | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Trial now transitioned) AT (Trial now transitioned) DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-020841-29 | Sponsor Protocol Number: ADAPT | Start Date*: 2011-07-07 | ||||||||||||||||
| Sponsor Name:King`s College London [...] | ||||||||||||||||||
| Full Title: The role of anti-IgE (omalizumab) in the management of severe recalcitrant paediatric atopic eczema | ||||||||||||||||||
| Medical condition: Severe eczema in children | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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