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Active clinical trials for "Thromboembolism"

Results 241-250 of 829

Peripheral Systemic Thrombolysis Versus Catheter Directed Thrombolysis for Submassive PE

Pulmonary EmbolismPulmonary Hypertension2 more

To determine whether peripheral low dose systemic thrombolysis (PLST) is non-inferior to catheter directed acoustic pulse thrombolysis (ACDT) in improving RV function and reducing pulmonary artery pressures in submassive pulmonary embolism (PE)

Completed29 enrollment criteria

PREvention of VENous ThromboEmbolism Following Radical Prostatectomy

Prostate CancerVenous Thromboembolism3 more

The PREVENTER Trial aims to compare the use of perioperative pharmacologic prophylaxis (subcutaneous heparin) with intermittent pneumatic compression devices (IPCs) to the use of IPCs alone for the prevention of venous thromboembolism (VTE) after radical prostatectomy (RP).

Terminated8 enrollment criteria

Mexican Multidisciplinary Registry of Patients With Venous Thromboembolic Disease

Venous ThromboembolismVenous Thrombosis1 more

REMMITE, a retrospective and prospective registry with one-year follow-up, will provide valuable insights into the clinical diagnosis, management, treatment trends as well as related outcomes of three cohorts: DVT, DVT-PE, PE patients throughout many regions of Mexico and through different health care systems.

Not yet recruiting5 enrollment criteria

Apixaban For Thromboprophylaxis In Patients With Acute Spinal Cord Injury

Spinal Cord InjuriesVenous Thromboembolism

Thromboprophylaxis options are limited for patients with acute spinal cord injury (SCI) and there are no studies on direct oral anticoagulants (DOACs) for thromboprophylaxis in this population. Participants will be randomized to apixaban 2.5 mg twice daily or standard dose low-molecular-weight heparin (LMWH), either enoxaparin 40 mg or dalteparin 5000 units, subcutaneously once daily for 90 days or until fully mobilized, whatever comes first. Thromboprophylaxis will be started as soon as hemostasis is achieved. The primary outcome for this pilot study will be the recruitment rate per year (i.e. the screened to enrolled ratio). The primary efficacy endpoint will be a composite of symptomatic, objectively verified, venous thromboembolism (VTE), defined as upper or lower limb deep vein thrombosis (DVT) and/or pulmonary embolism (PE) or sudden death where PE cannot be excluded. The primary safety endpoint will be major bleeding.

Terminated14 enrollment criteria

EINSTEIN Junior Phase II: Oral Rivaroxaban in Young Children With Venous Thrombosis

Venous Thromboembolism

The purpose of this study is to find out whether rivaroxaban is safe to use in children and how long it stays in the body. Safety will be assessed by looking at the incidence and types of bleeding events. There will also be a check for worsening of blood clots.

Completed16 enrollment criteria

Predictive Value of Whole Blood Coagulation Parameters for Post-discharge Venous Thromboembolism...

Venous Thromboembolism

This study plans to learn more about the role of 2 blood tests in predicting who might develop a blood clot in their arm or leg after major surgery. The investigators know that patients who have cancer and major surgery have a higher than normal risk of getting blood clots in the veins of their arms or legs. This can be very dangerous because the clot can move into your lungs.

Terminated3 enrollment criteria

Cancer Associated Thrombosis and Isoquercetin (CATIQ)

Thromboembolism of Vein VTE in Colorectal CancerThromboembolism of Vein in Pancreatic Cancer1 more

This research study is evaluating a drug called isoquercetin to prevent venous thrombosis (blood clots), in participants who have pancreas, non small cell lung cancer or colorectal cancer.

Completed31 enrollment criteria

Submassive and Massive Pulmonary Embolism Treatment With Ultrasound Accelerated Thrombolysis Therapy...

Pulmonary EmbolismAcute Pulmonary Embolism3 more

The purpose of this study is to determine if the EKOS EkoSonic® Endovascular Device when used in conjunction with recombinant tissue plasminogen activator (t-PA) as a treatment for acute PE will decrease the ratio of right ventricle (RV) to left ventricle (LV) diameter within 48 =/- 6 hours in participants with massive or submassive PE.

Completed23 enrollment criteria

Efficacy of Intermittent Pneumatic Compression (IPC) on Venous Thromboembolism Incidence in Intensive...

High Bleeding RiskHemorrhage

This multicentre open-label randomized parallel-group trial aims to evaluate the association intermittent pneumatic compression + elastick stockings versus elasting stockings alone on symptomatic or asymptomatic venous thromboembolism incidence, evaluated systematically at day 6 (+/-2days), in patients hospitalized in intensive care units and with high bleeding risk.

Completed18 enrollment criteria

Effectiveness of Bridging Anticoagulation for Surgery (The BRIDGE Study)

Arterial Thromboembolic EventsAtrial Fibrillation

Blood thinners, such as warfarin, prevent blood clots from forming, thereby reducing the risk of a stroke or heart attack. When people undergo surgery or certain procedures, they must stop using warfarin to prevent too much bleeding during and after the surgery or procedure. Some doctors prescribe a different blood thinner, one that works more quickly and wears off more quickly, to bridge the gap between starting and stopping warfarin. However, this short-term treatment is expensive, may increase the risk of bleeding, and has not been proven effective. This study will determine whether a bridging blood thinner called dalteparin is helpful or harmful for people with atrial fibrillation who stop taking warfarin in preparation for surgery or a procedure.

Completed28 enrollment criteria
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