- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Intraparenchymal hemorrhage.
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EudraCT Number: 2008-005653-37 | Sponsor Protocol Number: ICH-VKA | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Universityhospital of Heidelberg | |||||||||||||
Full Title: Multicenter, prospective randomized trial on the use of prothrombin complex and fresh frozen plasma in patients with intracerebral hemorrhage related to vitamin K antagonists (VKA) | |||||||||||||
Medical condition: Intracerebral hemorrhage (ICH) in patients related to vitamin K antagonists | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Suspended by CA) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002075-33 | Sponsor Protocol Number: ENRICH-AF | Start Date*: 2020-05-05 | ||||||||||||||||
Sponsor Name:Hamilton Health Sciences, through its Population Health Research Institute | ||||||||||||||||||
Full Title: Edoxaban for intracranial hemorrhage survivors with atrial fibrillation | ||||||||||||||||||
Medical condition: High risk atrial fibrillation patients with previous intracranial hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NO (Prematurely Ended) DE (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) SK (Trial now transitioned) DK (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004482-14 | Sponsor Protocol Number: P160917 | Start Date*: 2019-08-14 |
Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | ||
Full Title: Tocolysis in the management of preterm premature rupture of membranes before 34 weeks of gestation: a double-blinded randomized controlled trial | ||
Medical condition: Pregnant women with PPROM at 22 to 33 weeks gestation | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
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