- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: DVT prophylaxis.
Displaying page 1 of 3.
| EudraCT Number: 2005-004691-20 | Sponsor Protocol Number: BAY 59-7939/11357 | Start Date*: 2006-01-09 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: RECORD 2 Study: REgulation of Coagulation in ORthopedic Surgery to prevent DVT and PE, controlled, Double-Blind, Randomized Study of BAY59-7939 in the Extended Prevention of VTE in Patients Undergo... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) SE (Completed) LT (Completed) DK (Completed) EE (Completed) PT (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005090-20 | Sponsor Protocol Number: FADOI.01.2016 | Start Date*: 2018-05-17 | ||||||||||||||||
| Sponsor Name:FONDAZIONE FADOI | ||||||||||||||||||
| Full Title: Rivaroxaban or placebo for extended antithrombotic prophylaxis after laparoscopic surgery for colorectal cancer: a randomized, double blind, placebo-controlled study. THE PRO-LAPS STUDY II | ||||||||||||||||||
| Medical condition: Prevention of venous thromboembolism after laparoscopic surgery for colorectal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-004620-40 | Sponsor Protocol Number: BAY 59-7939/11356 | Start Date*: 2006-01-26 | |||||||||||
| Sponsor Name:Bayer HealthCare AS | |||||||||||||
| Full Title: RECORD 3 Study: REgulation of Coagulation in ORthopedic Surgery to Prevent DVT and PE; controlled, double-blind, randomized study of BAY 59-7939 in the prevention of VTE in subjects undergoing elec... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) SE (Completed) DE (Completed) DK (Completed) BE (Completed) ES (Completed) CZ (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002402-60 | Sponsor Protocol Number: BAY 59-7939/11355 | Start Date*: 2007-03-27 | |||||||||||
| Sponsor Name:Bayer Pharmaceutical | |||||||||||||
| Full Title: RECORD 4 Study: REgulation of Coagulation in ORthopedic Surgery to Prevent DVT and PE; a controlled, double-blind, randomized study of BAY 59-7939 in the prevention of VTE in subjects undergoing el... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) SE (Completed) DK (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004351-35 | Sponsor Protocol Number: BAY 59-7939/11354 | Start Date*: 2006-01-11 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: RECORD 1 Study: REgulation of Coagulation in ORthopedic Surgery to prevent DVT and PE, controlled, double-blind, randomized study of BAY 59-7939 in the extended prevention of VTE in patients underg... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) AT (Completed) DK (Completed) BE (Completed) LT (Completed) HU (Completed) SK (Completed) ES (Completed) IT (Completed) FI (Completed) CZ (Completed) DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004614-14 | Sponsor Protocol Number: BAY 59-7939/12839 | Start Date*: 2007-12-05 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: MAGELLaN - Multicenter, rAndomized, parallel Group Efficacy and safety study for the prevention of venous thromboembolism in hospitalized medically iLL patients comparing rivaroxabAN with enoxaparin | |||||||||||||
| Medical condition: Prevention of venous thromboembolism in patients who have been hospitalized for a medical illness | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) FR (Completed) DK (Completed) LT (Completed) GB (Completed) BE (Completed) AT (Completed) NL (Completed) ES (Completed) GR (Completed) PT (Completed) SI (Completed) SK (Completed) CZ (Completed) IT (Completed) PL (Completed) LV (Completed) FI (Completed) HU (Completed) EE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001630-21 | Sponsor Protocol Number: BAY59-7939/39039039STM4001/18262 | Start Date*: 2015-12-15 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: Efficacy and Safety of Rivaroxaban Prophylaxis Compared with Placebo in Ambulatory Cancer Patients Initiating Systemic Cancer Therapy and at High Risk for Venous Thromboembolism | |||||||||||||
| Medical condition: Venous thromboembolism (VTE) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) DE (Completed) CZ (Completed) BG (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023383-40 | Sponsor Protocol Number: TB-402-006 | Start Date*: 2011-02-15 | |||||||||||
| Sponsor Name:ThromboGenics N.V | |||||||||||||
| Full Title: Single Intravenous Administration of TB-402 for the Prophylaxis of Venous Thromboembolic Events (VTE) After Total Hip Replacement Surgery: A Phase IIb, Multicentre, Randomised, Active-Controlled, D... | |||||||||||||
| Medical condition: Venous Thromboembolic Event | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) LV (Completed) HU (Completed) AT (Completed) BG (Completed) NL (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001559-15 | Sponsor Protocol Number: CTO#2095 | Start Date*: 2022-11-11 | |||||||||||
| Sponsor Name:Ottawa Hospital Research Institute | |||||||||||||
| Full Title: StAtins for Venous Event Reduction in Patients with Venous Thromboembolism | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001954-40 | Sponsor Protocol Number: SPh/01/2014 | Start Date*: 2014-10-02 | |||||||||||
| Sponsor Name:SciencePharma spółka z ograniczoną odpowiedzialnością sp. k. | |||||||||||||
| Full Title: A randomized, multicenter, parallel, open-label study comparing the safety of the test investigational medicinal product (IMP) Enoxaparin Sodium 40 with the reference IMP Clexane for the prevention... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism (VTE) in patients undergoing high VTE-risk knee surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003674-96 | Sponsor Protocol Number: CV185-036 | Start Date*: 2007-07-27 | |||||||||||||||||||||
| Sponsor Name:Bristol Myers Squibb | |||||||||||||||||||||||
| Full Title: A Phase 3 Randomized, Double-blind, Parallel-group, Multi-center Study of the Safety and Efficacy of Apixaban for Prophylaxis of Venous Thromboembolism in Acutely Ill Medical Subjects During and Fo... | |||||||||||||||||||||||
| Medical condition: Total Venous thromboembolism (VTE), defined as the combination of fatal or nonfatal pulmonary embolism, symptomatic deep vein thrombosis (DVT), and asymptomatic proximal DVT. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) SE (Completed) NL (Completed) CZ (Completed) AT (Completed) FR (Completed) DK (Completed) HU (Completed) DE (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-002681-31 | Sponsor Protocol Number: BAY1213790/17664 | Start Date*: 2017-07-13 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: A randomized, active-comparator-controlled, multicenter study to assess the safety and efficacy of different doses of BAY 1213790 for the prevention of venous thromboembolism in patients undergoing... | |||||||||||||
| Medical condition: Prevention of venous thromboembolism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) LT (Completed) CZ (Completed) DE (Completed) LV (Completed) BG (Completed) PL (Completed) GR (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004539-39 | Sponsor Protocol Number: TB-402-004 | Start Date*: 2008-12-19 | |||||||||||
| Sponsor Name:ThromboGenics N.V | |||||||||||||
| Full Title: Single Intravenous Administration of TB-402 for the Prophylaxis of Venous hromboembolic Events (VTE) After Total Knee Replacement Surgery: A Dose-Escalating, Multicenter, Randomised, Active-Control... | |||||||||||||
| Medical condition: Venous thrombolic events | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-002586-12 | Sponsor Protocol Number: 1160.63 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: Twice-daily oral direct thrombin inhibitor dabigatran in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary embo... | |||||||||||||
| Medical condition: long-term prevention of recurrent symptomatic venous thromboembolism (VTE) in patients with symptomatic deep-vein thrombosis (DVT) or pulmonary embolism (PE) who completed 6 to 18 months of treatme... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) AT (Completed) IT (Completed) PL (Completed) CZ (Completed) NL (Completed) BE (Completed) LT (Completed) LV (Completed) EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000305-13 | Sponsor Protocol Number: RIVAROXDVT3002/BAY59-7939/17261 | Start Date*: 2014-07-07 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: Medically Ill Patient Assessment of Rivaroxaban Versus Placebo IN Reducing Post-Discharge Venous Thrombo-Embolism Risk (MARINER) | |||||||||||||
| Medical condition: Prevention of symptomatic venous thromboembolism (VTE) and VTE-related death posthospital discharge in high-risk, medically ill patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) HU (Completed) CZ (Completed) IT (Completed) ES (Completed) NL (Completed) LT (Completed) BG (Completed) GR (Completed) LV (Completed) AT (Completed) DE (Completed) GB (Completed) PT (Completed) SK (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007942-36 | Sponsor Protocol Number: EFC6520 | Start Date*: 2008-09-30 | |||||||||||
| Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
| Full Title: A Multinational, Multicenter, Randomized, Double Blind Study comparing the Efficacy and Safety of AVE5026 with enoxaparin for the Prevention of Venous Thromboembolism in Patients Undergoing Major A... | |||||||||||||
| Medical condition: The subjects who will participate to this clinical trial are patients undergoing major abdominal surgery. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) LV (Completed) EE (Completed) DK (Completed) BE (Completed) SE (Completed) HU (Completed) CZ (Completed) LT (Completed) SI (Completed) IT (Completed) SK (Completed) BG (Completed) AT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004676-12 | Sponsor Protocol Number: CMEX839BDE03 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Novartis Pharma GmbH | ||
| Full Title: A randomized, double-blind, multi-center comparison of the efficacy and safety of certoparin (3000 U anti-Xa o.d.) with unfractionated heparin (5000 IU t.i.d.) in the prophylaxis of thromboembolic ... | ||
| Medical condition: acutely ill immobilized medical patients | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004494-96 | Sponsor Protocol Number: BAY 59-7939/IMP 11899 | Start Date*: 2007-03-19 |
| Sponsor Name:Bayer HealthCare AG | ||
| Full Title: Once-daily oral direct factor Xa inhibitor rivaroxaban in the long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary emb... | ||
| Medical condition: Long-term prevention of recurrent symptomatic venous thromboembolism in patients with symptomatic deep-vein thrombosis or pulmonary embolism. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) ES (Completed) SE (Completed) DE (Completed) FI (Completed) FR (Completed) HU (Completed) AT (Completed) IT (Completed) DK (Completed) CZ (Completed) NL (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001341-14 | Sponsor Protocol Number: BAY 59-7939 / 11527 | Start Date*: 2004-11-04 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: Controlled, Double-Blind, Randomized, Dose-ranging Study of once-daily regimen of BAY59-7939 in the Prevention of VTE in Patients Undergoing Elective Total Hip Replacement-ODIXaHIP-OD Study | |||||||||||||
| Medical condition: Deep Venous Thrombosis prophylaxis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) SE (Completed) AT (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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) | |||||||||||||
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