- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: livedo.
Displaying page 1 of 1.
EudraCT Number: 2012-000108-13 | Sponsor Protocol Number: UKM10_0018 | Start Date*: 2012-12-27 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: A phase II multicenter trial with Rivaroxaban in the treatment of livedoid vasculopathy assessing the pain on a visual analog scale (VAS) | ||
Medical condition: Treatment of livedoid vasculopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002751-15 | Sponsor Protocol Number: ST-001 | Start Date*: 2019-04-20 | |||||||||||
Sponsor Name:Hope Pharmaceuticals Ltd | |||||||||||||
Full Title: A Phase 3, Intravenous Sodium Thiosulfate for Acute Calciphylaxis Treatment: A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial | |||||||||||||
Medical condition: Calciphylaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004668-71 | Sponsor Protocol Number: 11/0499 | Start Date*: 2014-09-25 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: An Open Label Randomised Controlled Trial of Mycophenolate Mofetil Versus Cyclophosphamide for the Induction of Remission of Childhood Polyarteritis Nodosa | |||||||||||||
Medical condition: Childhood systemic polyarteritis nodosa (PAN) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) PT (Completed) ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001131-36 | Sponsor Protocol Number: OS320-3005 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Osmotica Pharmaceutical Corp. | |||||||||||||
Full Title: A Multicenter, Randomized, Placebo-controlled, Double-blind, 16 Week Study to Evaluate the Efficacy and Safety of Amantadine HCl Extended Release Tablets in Parkinson's Disease Subjects with Levodo... | |||||||||||||
Medical condition: Parkinson's Disease Subjects with Levodopa-Induced Dyskinesias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001132-10 | Sponsor Protocol Number: OS320-3006 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:Osmotica Pharmaceutical Corp. | |||||||||||||
Full Title: A Multicenter, Randomized, Placebo-controlled, Double-blind, 26 Week Study to Evaluate the Efficacy and Safety of Amantadine HCl Extended Release Tablets in Parkinson's Disease Subjects with Levodo... | |||||||||||||
Medical condition: Parkinson's Disease Subjects with Levodopa-Induced Dyskinesias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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