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Nadroparin

DRUG15 trials

Sponsors

Universitair Medisch Centrum Groningen, Onze Lieve Vrouwe Gasthuis, University Hospital, Geneva, GlaxoSmithKline, Beijing Chao Yang Hospital

Conditions

Acute Ischemic StrokeAll patients who receive ECMO treatment during the study period in one the participating centers from which (deferred) informed consent is obtained. Patients in whom the ECMO is only used to bridge a procedure like a high risk percutaneous coronary intervention or during surgery are excluded.Anticoagulants and Bleeding DisordersBypass ComplicationsCOVID-19CancerDeep Vein ThrombosisEndstage Renal Disease

Phase 2

Phase 3

Effects Of Nadroparin In Patients With Lung, Pancreas Or Prostate Cancer
CompletedNCT00312013
GlaxoSmithKlineThrombosis, Venous
Start: 2006-05-31End: 2009-07-31Updated: 2017-03-23
A Study to Evaluate the Efficacy and Safety of Fondaparinux for the Prevention of Venous Blood Clots in Patients With a Plaster Cast or Other Type of Immobilization for a Below-knee Injury Not Needing Surgery
CompletedNCT00843492
GlaxoSmithKlineThrombosis, Venous
Start: 2008-12-31End: 2010-06-30Updated: 2016-03-16
Safety of DAbigatran and RIvaroxaban Versus NAdroparin in the Prevention of Venous Thromboembolism After Knee Arthroplasty Surgery
CompletedNCT01431456
Martini Hospital GroningenVenous Thromboembolism
Start: 2013-09-30End: 2014-10-31Updated: 2018-06-07
Rivaroxaban and Vitamin K Antagonists for the Anticoagulation for the Implantation of Vena Cava Filters
RecruitingNCT04066764
Second Affiliated Hospital, School of Medicine, Zhejiang UniversityVenous Thromboembolism
Start: 2020-05-08End: 2024-10-01Target: 200Updated: 2024-04-18
Rivaroxaban for the Prevention of Deep Vein Thrombosis in Patients With Left Iliac Vein Compression - The PLICTS Study
RecruitingNCT04067505
Second Affiliated Hospital, School of Medicine, Zhejiang UniversityMay-Thurner Syndrome
Start: 2020-05-18End: 2024-12-31Target: 224Updated: 2024-04-18
Reduced anticoagulation targets in extracorporeal life support
Not yet recruitingCTIS2023-509675-16-01
Universitair Medisch Centrum GroningenAll patients who receive ECMO treatment during the study period in one the participating centers from which (deferred) informed consent is obtained. Patients in whom the ECMO is only used to bridge a procedure like a high risk percutaneous coronary intervention or during surgery are excluded.
Target: 330Updated: 2025-01-28

Phase 4

Unknown Phase

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