- Trials with a EudraCT protocol (123)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
123 result(s) found for: Enoxaparin.
Displaying page 1 of 7.
EudraCT Number: 2020-001823-15 | Sponsor Protocol Number: 20CH089 | Start Date*: 2020-04-28 | ||||||||||||||||
Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
Full Title: Evaluation of the concentration-effect relationship of enoxaparin for thromboembolic prevention in COVID-19 resuscitation patients. COV-ENOX study | ||||||||||||||||||
Medical condition: covid-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-006113-40 | Sponsor Protocol Number: KARD-12-2005 | Start Date*: 2006-05-03 |
Sponsor Name:Universitäres Herzzentrum Hamburg | ||
Full Title: Untersuchung der Modulation der Endothelfunktion durch Enoxaparin bei Patienten mit Koronarkrankheit. Bedeutung der Enoxaparin-vermittelten Dissoziation endothelial gebundener Oxidasen für die Regu... | ||
Medical condition: Stabile koronare Herzerkrankung | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001127-24 | Sponsor Protocol Number: 290115-1 | Start Date*: 2015-06-03 |
Sponsor Name:Tampere Heart Hospital | ||
Full Title: Pharmacokinetics of enoxaparin after coronary artery bypass graft surgery | ||
Medical condition: Thromboprophylaxis after coronary artery bypass graft surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000099-12 | Sponsor Protocol Number: APHP180617 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: Dose-adjustment of enoxaparin by a bayesian pharmacological approach in pediatric renal transplant recipients | |||||||||||||
Medical condition: Allograft vascular thrombosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002214-40 | Sponsor Protocol Number: HLS-02COVID19/2020 | Start Date*: 2020-05-20 |
Sponsor Name:ASST FATEBENEFRATELLI SACCO | ||
Full Title: ENOXAPARIN AT PROPHYLACTIC OR THERAPEUTIC DOSES WITH MONITORING OF OUTCOMES IN SUBJECTS INFECTED WITH COVID-19: PILOT STUDY ON 300 CASES ENROLLED AT ASST FBF SACCO | ||
Medical condition: SARS-CoV-2 related pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001708-41 | Sponsor Protocol Number: X-COVID19 | Start Date*: 2020-04-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA AO OSPEDALE NIGUARDA CA' GRANDA | |||||||||||||
Full Title: Enoxaparin for thromboprophylaxis in hospitalized COVID-19 patients: comparison of 40 mg o.d. versus 40 mg b.i.d. A randomized Clinical Trial | |||||||||||||
Medical condition: SARS-CoV-2 Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000485-29 | Sponsor Protocol Number: STH19752 | Start Date*: 2017-05-23 |
Sponsor Name:Dr | ||
Full Title: Prolonged ENoxapariN in primarY Percutaneous Coronary Intervention; a Pilot Pharmacodynamic study (PENNY PCI study) | ||
Medical condition: ST elevation myocardial infarction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002259-20 | Sponsor Protocol Number: CASUAL_ECMO | Start Date*: 2023-08-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: A three-arm randomized controlled non-inferiority pilot study Comparing Anticoagulation Strategies using Unfractionated heparin, Argatroban and Low-molecular-weight heparin for Extracorporeal Memb... | ||
Medical condition: patients with indication for extracorporeal membrane oxygenation therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003125-39 | Sponsor Protocol Number: TRI-08892 | Start Date*: 2020-10-12 |
Sponsor Name:Thrombosis Research Institute | ||
Full Title: Early thromboprophylaxis in COVID-19 (ETHIC trial): an open label, randomized phase IIIb trial of community-based prophylactic low-molecular-weight heparin (LMWH) versus standard of care (no enoxap... | ||
Medical condition: Confirmed diagnosis of SARS-CoV-2 with symptomatic COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) | ||
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: 2004-001128-19 | Sponsor Protocol Number: CV185-010 | Start Date*: 2004-11-02 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: A Phase 2 Randomized, Double Blinded (BMS-562247 and enoxaparin), Active-Controlled (enoxaparin and warfarin), Parallel-Arm, Dose Response Study of the Oral Factor Xa Inhibitor BMS-562247 in Subjec... | ||
Medical condition: Prevention of asymptomatic and symptomatic deep vein thrombosis (DVT) and non-fatal pulmonary embolism (PE) in subjects undergoing knee replacement surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000315-76 | Sponsor Protocol Number: 1375_RCF_MAC | Start Date*: 2021-12-06 | |||||||||||
Sponsor Name:Centro Hospitalar Universitário de Lisboa Central, EPE | |||||||||||||
Full Title: Low molecular weight heparin in the treatment of early fetal growth restriction | |||||||||||||
Medical condition: Early fetal growth restriction | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2020-005624-10 | Sponsor Protocol Number: OVID-trial | Start Date*: 2021-05-06 | ||||||||||||||||
Sponsor Name:University Hospital Zurich | ||||||||||||||||||
Full Title: ENOXAPARIN FOR PRIMARY THROMBOPROPHYLAXIS IN AMBULATORY PATIENTS WITH CORONAVIRUS: THE MULTICENTER RANDOMIZED CONTROLLED OVID TRIAL | ||||||||||||||||||
Medical condition: Patients diagnosed with COVID-19, a novel viral disease characterized by severe systemic, pulmonary, and vessel inflammation and coagulation activation. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003148-21 | Sponsor Protocol Number: DU176b-F-E308 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Daiichi Sankyo Development Ltd | |||||||||||||
Full Title: A prospective, randomised, open-label, blinded endpoint evaluation (PROBE) parallel group study comparing edoxaban (DU-176b) with enoxaparin/warfarin followed by warfarin alone in subjects undergoi... | |||||||||||||
Medical condition: Stroke and thromboembolism prevention in patients with non-valvular atrial fibrillation (NVAF) undergoing planned electrical cardioversion. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) DE (Completed) GB (Completed) HU (Completed) IT (Completed) DK (Completed) ES (Completed) AT (Completed) CZ (Completed) NL (Completed) RO (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003122-88 | Sponsor Protocol Number: SELK2-00005 | Start Date*: 2019-01-21 | |||||||||||
Sponsor Name:Tetherex Pharmaceuticals Corporation | |||||||||||||
Full Title: A Phase 2, Randomized, Active Comparator-Controlled, Open-Label, Adaptive Design Study to Assess the Safety and Efficacy of Intravenously-Administered SelK2 in Patients Undergoing Total Knee Arthro... | |||||||||||||
Medical condition: Venous thromboembolism occurring in patients undergoing total knee replacement arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) BG (Completed) LT (Completed) PL (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: 2007-003746-15 | Sponsor Protocol Number: 259-4-111IIT-ARX0257 | Start Date*: 2008-03-27 | |||||||||||
Sponsor Name:Ammerland-Klinik Westerstede | |||||||||||||
Full Title: prospective randomized open study on the comparison of fondaparinux with the low-molecular-weight heparin enoxaparin in patients undergoing femoro-distal venous bypass operation | |||||||||||||
Medical condition: Patients with underlying peripheral occlusive vascular disease undergoing bypass surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003756-37 | Sponsor Protocol Number: ANT-005 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:Anthos Therapeutics | |||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Blinded Endpoint Evaluation, Active-Controlled, Dose-Ranging Study to Compare the Efficacy and Safety of i.v. MAA868 and s.c. Enoxaparin in Adult Patients Und... | |||||||||||||
Medical condition: Elective unilateral total knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) BE (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005433-30 | Sponsor Protocol Number: ENOXA-NSCLC | Start Date*: 2009-01-29 |
Sponsor Name:Medizinische Hochschule Hannover, Klinik für Pneumologie | ||
Full Title: Taxotere-Enoxaparin-(ENOXA)-Studie: 1st-Line Docetaxel-Platin Chemotherapie alleine oder in Kombination mit Enoxaparin bei Patienten mit lokal fortgeschrittenem oder metastasiertem nicht-kleinzelli... | ||
Medical condition: Patienten mit lokal fortgeschrittenem oder metastasiertem nicht-kleinzelligem Bronchial-Karzinom Stadium IIIb (inoperabel)/IV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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