- Trials with a EudraCT protocol (634)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (39)
634 result(s) found for: Deep.
Displaying page 1 of 32.
EudraCT Number: 2007-003762-18 | Sponsor Protocol Number: 2007.468/11 | Start Date*: 2008-10-23 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Prospective monocenter accuracy study of Vasovist contrast enhanced magnetic resonance venography (CE-MRV) to detect venous thrombi in patients with Ultrasonography detected peripheral acute deep ... | |||||||||||||
Medical condition: Acute deep vein thrombosis (DVT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004826-28 | Sponsor Protocol Number: ict-bem-2004-02 | Start Date*: 2005-03-28 | |||||||||||
Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
Full Title: Multicenter double-blind placebo controlled aleatorized study to evaluate the efficacy and safety of bemiparin (3500 IU/day) in thromboprophylaxis in cancer paients with central vein catheter | |||||||||||||
Medical condition: Deep Vein Thrombosis related central vein catheter (DVT-CVC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005524-13 | Sponsor Protocol Number: I-ICRNS-005-PRCLD-DVT-01 | Start Date*: 2006-03-22 | |||||||||||
Sponsor Name:CRINOS S.p.A. | |||||||||||||
Full Title: Defibrotide in the prevention of recurrences in venous thrombosis: DEPRIVE. A randomised, multicentre, European, double blind, parallel group study, to assess the efficacy and tolerability of defib... | |||||||||||||
Medical condition: DVT and PE are part of the same disease that can be defined Venous Thromboembolism (VTE). Treatment of the acute phases is well established: LMWH during the first days and OAT for 3-12 months. Afte... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002270-29 | Sponsor Protocol Number: IN 0401 INT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Safety profile of innohep versus subcutaneous unfractionated Heparin in elderly patients with impaired renal function treated for acute deep vein thrombosis | |||||||||||||
Medical condition: Treatment of acute deep vein thrombosis in elderly patients with impaired renal function | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) DK (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005326-30 | Sponsor Protocol Number: EFC5945 | Start Date*: 2006-05-19 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: International, multicenter, randomized, parallel group, double-blind study, in patients with acute symptomatic deep vein thrombosis of the lower limbs, demonstrating the bioequipotency at steady st... | |||||||||||||
Medical condition: Patients with confirmed acute symptomatic DVT of the lower limbs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DK (Completed) BE (Completed) ES (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001083-43 | Sponsor Protocol Number: BAY 59-7939 / 11223 | Start Date*: 2004-11-23 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Oral Direct Factor Xa Inhibitor BAY 59-7939 in Patients with acute symptomatic Deep Vein Thrombosis ODIXa-DVT A prospective, randomized, multinational, multicenter, partially blinded, parallel-grou... | |||||||||||||
Medical condition: Acute deep vein thrombosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002340-32 | Sponsor Protocol Number: APIDULCIS | Start Date*: 2019-03-19 | ||||||||||||||||
Sponsor Name:FONDAZIONE ARIANNA ANTICOAGULAZIONE | ||||||||||||||||||
Full Title: APIDULCIS: Extended anticoagulation with low-dose apixaban after a standard course anticoagulation in patients with a first venous thromboembolism who have positive d-dimer | ||||||||||||||||||
Medical condition: a first episode of proximal deep vein thrombosis (DVT) and/or pulmonary embolism (PE) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002171-16 | Sponsor Protocol Number: BAY 59-7939 / 11528 | Start Date*: 2005-01-10 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Once-daily oral Direct Factor Xa Inhibitor BAY 59-7939 in Patients with acute symptomatic Deep Vein Thrombosis. The Einstein-DVT dose-finding study. | |||||||||||||
Medical condition: Acute syntomatic deep vein thrombosis | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000170-97 | Sponsor Protocol Number: 2023-01-1200-01 | Start Date*: 2023-06-30 | |||||||||||
Sponsor Name:LMU Universitätsklinikum München | |||||||||||||
Full Title: A single dose of apixaban for the prevention of thrombotic events in the context of long-distance flights | |||||||||||||
Medical condition: Symptomatic leg vein thrombosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005695-32 | Sponsor Protocol Number: FRIAT-BEM-2005-01 | Start Date*: 2006-03-10 | |||||||||||
Sponsor Name:Fundación Renal Iñigo Álvarez de Toledo | |||||||||||||
Full Title: Ensayo clínico aleatorizado, controlado y abierto, para evaluar la eficacia (biocompatibilidad peritoneal) de la adición de bemiparina a la solución de icodextrina, en pacientes en diálisis periton... | |||||||||||||
Medical condition: Pacientes con insuficiencia renal en tratamiento con diálisis peritoneal y trastornos de la función peritoneal. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005351-14 | Sponsor Protocol Number: CV185-035 | Start Date*: 2007-05-29 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Active-controlled, Parallel-group, Multi-center Study to Evaluate the Safety and Efficacy of Apixaban in Subjects Undergoing Elective Total Hip Replacement Surg... | ||||||||||||||||||
Medical condition: Subjects undergoing elective total hip replacement (THR) surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) FR (Completed) BE (Completed) GB (Completed) DK (Completed) HU (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004953-27 | Sponsor Protocol Number: CV185-057 | Start Date*: 2008-07-29 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A SAFETY AND EFFICACY TRIAL EVALUATING THE USE OF APIXABAN FOR THE EXTENDED TREATMENT OF DEEP VEIN THROMBOSIS AND PULMONARY EMBOLISM (Apixaban after the initial Management of PuLmonary embolIsm an... | ||||||||||||||||||
Medical condition: Venous Thromboembolism (VTE) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) PT (Completed) GB (Completed) AT (Completed) DK (Completed) CZ (Completed) IT (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001813-17 | Sponsor Protocol Number: R1282 | Start Date*: 2012-08-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||||||||||||||||||||||||||||||||||||||
Full Title: Study of apoptosis related changes and endothelial responses of multiple myeloma patients treated with chemotherapy. | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chemotherapy related thrombosis in patients treated for multiple myeloma. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016992-31 | Sponsor Protocol Number: COU-001A | Start Date*: 2010-03-19 | |||||||||||||||||||||
Sponsor Name:Democritus Universityof Thrace Medical School [...] | |||||||||||||||||||||||
Full Title: EUropean Pharmacogenetics of AntiCoagulation Therapy trial | |||||||||||||||||||||||
Medical condition: Newly diagnosed patients with venous tromboembolism (VTE) or atrial fibrillation (AF) requiring oral anticoagulation with phenprocoumon. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016993-34 | Sponsor Protocol Number: COU-001W | Start Date*: 2010-09-02 | |||||||||||||||||||||
Sponsor Name:Uppsala University Hospital | |||||||||||||||||||||||
Full Title: EUropean Pharmacogenetics of AntiCoagulation Therapy trial | |||||||||||||||||||||||
Medical condition: Newly diagnosed patients with venous tromboembolism (VTE) or atrial fibrillation (AF) requiring oral anticoagulation with warfarin. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005162-29 | Sponsor Protocol Number: RivaSVT100 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:A.O. OSPEDALE DI CIRCOLO E FONDAZIONE MACCHI | |||||||||||||
Full Title: Treatment of portal, mesenteric, and splenic vein thrombosis with rivaroxaban. A pilot, prospective cohort study | |||||||||||||
Medical condition: Portal, mesenteric, and splenic vein thrombosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006896-19 | Sponsor Protocol Number: CV185-047 | Start Date*: 2007-09-06 | |||||||||||||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Active-controlled (Enoxaparin 40 mg QD), Parallel-group, Multi-center Study to Evaluate the Safety and Efficacy of Apixaban in Subjects Undergoing Elective Tota... | |||||||||||||||||||||||
Medical condition: Venous Thromboembolic Events | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) NL (Completed) AT (Completed) BE (Completed) FR (Completed) HU (Completed) SE (Completed) IT (Completed) CZ (Completed) DK (Completed) DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016994-13 | Sponsor Protocol Number: COU-001P | Start Date*: 2010-03-19 | |||||||||||||||||||||
Sponsor Name:University Utrecht [...] | |||||||||||||||||||||||
Full Title: EUropean Pharmacogenetics of AntiCoagulation Therapy trial | |||||||||||||||||||||||
Medical condition: Newly diagnosed patients with venous tromboembolism (VTE) or atrial fibrillation (AF) requiring oral anticoagulation with phenprocoumon. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) AT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015336-15 | Sponsor Protocol Number: 29462 | Start Date*: 2009-09-30 | |||||||||||
Sponsor Name:Department of Vascular Medicine of the Academic Medical Center | |||||||||||||
Full Title: Long-term treatment for cancer patients with deep vein thrombosis or pulmonary embolism - a randomized open label study | |||||||||||||
Medical condition: Deep venous thrombosis or pulmonary embolism in patients with cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) IT (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000619-26 | Sponsor Protocol Number: BAY59-7939/16416 | Start Date*: 2014-06-11 | ||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||||||||||||
Full Title: Reduced-dosed rivaroxaban and standard-dosed rivaroxaban versus ASA in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis and... | ||||||||||||||||||||||||||||
Medical condition: Long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis and/or pulmonary embolism | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) SE (Completed) AT (Completed) IT (Completed) ES (Completed) GB (Completed) CZ (Completed) DE (Completed) HU (Completed) DK (Completed) NL (Completed) NO (Completed) PL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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