- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Propylene glycol.
Displaying page 1 of 1.
EudraCT Number: 2008-005890-37 | Sponsor Protocol Number: K201-I/280301BS | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: Assessment of the effects on barrier impairment, clinical features and bacterial colonization of topical formulations in patients with atopic eczema; a phase IIa, single-center, randomized, observe... | |||||||||||||
Medical condition: To assess the barrier impairment, clinical skin condition and bacterial colonization in patients with atopic eczema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005242-36 | Sponsor Protocol Number: K40-3 | Start Date*: 2006-12-13 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A multicenter, randomised, double-blind, placebo-controlled clinical study evaluating efficacy, safety and tolerability of topical K40 in 8 weeks treatment of adult patients with moderate to severe... | |||||||||||||
Medical condition: Seborrhoeic Dermatitis of the scalp. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002325-31 | Sponsor Protocol Number: 11.105 | Start Date*: 2005-11-04 |
Sponsor Name:Taunton & Somerset NHS Trust | ||
Full Title: Two parallel trials to compare the effectiveness, and potential adverse side-effects, of four routinely used topical therapies to prolong breastfeeding, by either (1) preventing or (2) treating nip... | ||
Medical condition: Nipple pain in breastfeeding women | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004979-37 | Sponsor Protocol Number: 06-004 | Start Date*: 2006-10-27 |
Sponsor Name:MediQuest Therapeutics, Inc. | ||
Full Title: Phase III “In-Life” Study of a Topical Gel Formulation of Nitroglycerin, MQX-503, and Matching Placebo Gel in the Treatment and Prevention of Raynaud’s Phenomenon | ||
Medical condition: Moderate to severe primary Raynaud’s, OR patients with Raynaud’s phenomenon secondary to autoimmune diseases, such as scleroderma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001725-75 | Sponsor Protocol Number: 2015-DFU-301 | Start Date*: 2018-12-12 |
Sponsor Name:FirstString Research, Inc. | ||
Full Title: A Phase 3, Randomized, Double-blind, Parallel-group, Vehicle controlled, Multicenter Study of the Efficacy and Safety of Granexin Gel in the Treatment of Diabetic Foot Ulcer (GAIT 1) | ||
Medical condition: Diabetic Foot Ulcer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006188-59 | Sponsor Protocol Number: K301-1 | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: A multicenter, randomised double blind, placebo-controlled study of efficacy, safety and tolerability of Kaprolac® K301 for the treatment of seborrhoeic eczema (SE) of the scalp. | |||||||||||||
Medical condition: seborrhoeic dermatitis of the scalp | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022622-32 | Sponsor Protocol Number: MOB015-I | Start Date*: 2010-11-11 | |||||||||||
Sponsor Name:Moberg Derma AB | |||||||||||||
Full Title: An open, multi-centre trial comparing the efficacy and safety of two different treatment regimens of topical MOB015 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) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003901-93 | Sponsor Protocol Number: RC2019.1.6_GIAQUINTO | Start Date*: 2020-05-27 | |||||||||||
Sponsor Name:IRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA | |||||||||||||
Full Title: Monocentric, indipendent, phase II clinical trial, randomized in open to three different lZ delivery sequences in pediatric patients aged 1 and 12, in intensive care and mechanically ventilated. | |||||||||||||
Medical condition: Critical patients subjected to mechanical ventilation and hospitalized in PICU | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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