- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Lepirudin.
Displaying page 1 of 1.
| EudraCT Number: 2007-000564-25 | Sponsor Protocol Number: FLHIT | Start Date*: 2007-04-04 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: Fondaparinux vs Lepirudin in the treatment of heparin-induced thrombocytopenia, with or without thrombosis. A multicenter, randomized, parallel group study of treatment with fondaparinux (7.5 mg s... | |||||||||||||
| Medical condition: thrombocytopenia heparin-induced | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003122-28 | Sponsor Protocol Number: ArgLepi-2006 | Start Date*: 2008-12-19 | |||||||||||
| Sponsor Name:Heinrich-Heine-Universität Düsseldorf | |||||||||||||
| Full Title: Argatroban versus Lepirudin in Critically Ill Patients | |||||||||||||
| Medical condition: Critically ill patients are usually treated with heparin for anticoagulation. A serious complication of heparin therapy is heparin-induced thrombocytopenia type II (HIT). Patients with HIT have t... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000730-42 | Sponsor Protocol Number: ARG-E07 | Start Date*: 2009-01-09 | |||||||||||
| Sponsor Name:Mitsubishi Tanabe Pharma Corporation | |||||||||||||
| Full Title: An open-label, multi-centre, clinical study to collect information on the clinical use of argatroban in patients with heparin induced thrombocytopenia (HIT) Type II who require parenteral antithrom... | |||||||||||||
| Medical condition: Heparin induced thrombocytopenia (HIT) Type II | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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