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Venous Thrombosis clinical trials

View clinical trials related to Venous Thrombosis.

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NCT ID: NCT02651909 Completed - Anemia Clinical Trials

Utilization of TEG to Monitor Rivaroxaban Activity

Start date: April 2016
Phase:
Study type: Observational

The invesigators seek to devise a strategy for the assessment of Rivaroxaban activity in trauma and Emergency General Surgery (EGS) patients available as point-of-care testing. Thromboelastography (TEG) is a point of care, viscoelastic measurement of coagulation that is widely used in trauma and is viewed by many as superior to standard coagulation studies for the assessment of coagulopathy following injury and may be useful in detecting rivaroxaban effect in trauma and EGS patients to assess the degree of functional factor Xa impairment.

NCT ID: NCT02600260 Completed - Pulmonary Embolism Clinical Trials

Thromboprophylaxis in Pregnant Women in Hospital: A Prospective Clinical Trial

Start date: December 1, 2014
Phase: N/A
Study type: Interventional

Hospitalization in pregnancy and childbirth greatly increases the thromboembolic risk of these patients. The application of a protocol for assessing the risk of VTE reduces mortality and morbidity of these phenomena.

NCT ID: NCT02598609 Completed - Clinical trials for Intubation Complication

SEPREVEN: a Stepped-wedge Randomised Controlled Trial

SEPREVEN
Start date: November 23, 2015
Phase: N/A
Study type: Interventional

Adverse events are frequent in Neonatal Intensive Care Units' (NICU) patients and account for a high morbidity and mortality. Possible severe adverse events are central line associated bloodstream infections (CLABSI), ventilator and catheter associated adverse events and medication errors. Severity of the patient's outcome after an adverse event can be classified using the National Coordinating Council for Medication Error Reporting and Preventing (NCC MERP) Index for categorizing medication errors. The study will test the hypothesis that rates of adverse events in NICU patients will be reduced by the implementation of an educational program for the NICU caregivers (nurses and physicians), consisting of strategies for recognizing and preventing adverse events in their unit. These strategies will be oriented to prevent CLABSI, medication errors, skin and nasal complications and ventilator and catheter-associated adverse events. This trial has a stepped wedge cluster design, in which the NICUs from 12 hospitals in France will be randomized to the timing of implementation of the educational program. In order to describe the adverse events occurring during the study period, an anonymous voluntary adverse event reporting system will be provided to the caregivers of the participating units. A nested study will examine how caregivers communicate with the patients' parents in case of adverse event (disclosure or not, and caregivers' reasons). The rates of adverse events will be measured retrospectively using a neonatal NICU trigger tool.

NCT ID: NCT02585713 Completed - Pulmonary Embolism Clinical Trials

Apixaban or Dalteparin in Reducing Blood Clots in Patients With Cancer Related Venous Thromboembolism

Start date: November 20, 2015
Phase: Phase 3
Study type: Interventional

This randomized phase III trial studies the side effects of and compares apixaban and dalteparin in reducing blood clots in patients with cancer-related venous thromboembolism. Venous thromboembolism is a condition in which a blood clot forms in a vein and then breaks off and moves through the bloodstream. Patients with cancer are at increased risk for venous thromboembolism. Apixaban and dalteparin are drugs used to prevent blood clots from forming or to treat blood clots that have formed. It is not yet known whether apixaban or dalteparin is more effective in reducing blood clots in patients with cancer related venous thromboembolism. ADAM-VTE

NCT ID: NCT02584842 Completed - Bleeding Clinical Trials

Rivaroxaban in Endovenous Laser Ablation With and Without Miniphlebectomy

RITE
Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine retrospectively if the application of rivaroxaban after endovenous laser ablation with and without miniphlebectomy is safe and if it lowers the risk of venous thrombosis.

NCT ID: NCT02581176 Completed - Neoplasms Clinical Trials

Apixaban as Treatment of Venous Thrombosis in Patients With Cancer: The CAP Study

CAP
Start date: April 2016
Phase: Phase 4
Study type: Interventional

This study is a single-arm, phase IV trial, of apixaban as treatment of venous thrombosis in patients with cancer. The current standard treatment of venous thrombosis in cancer patients is subcutaneous injections with low molecular weight heparin. During the last 5 years several new direct acting oral anticoagulants have been tested out as treatment of venous thrombosis. But very few cancer patients were included in the phase III clinical trials of the direct acting oral anticoagulants. Thus, there is a lack of information on how cancer patients with venous thrombosis will respond to treatment with direct acting oral anticoagulants. The current study will investigate the direct acting oral anticoagulant apixaban in cancer patients with venous thrombosis.

NCT ID: NCT02567903 Completed - Venous Thrombosis Clinical Trials

Tourniquet Study: A Clinical Trial Into the Effect of Tourniquet Use on the Coagulation System

Start date: September 2015
Phase: N/A
Study type: Interventional

Knee arthroscopy is the most commonly performed orthopaedic procedure worldwide, with, according to the American Society for Sports Medicine, over 4 million procedures performed each year. The risk of venous thrombosis following this procedure is considerable with rates of symptomatic events varying between 0.9% and 4.6%. It is currently unknown how this high risk comes about considering its short duration and minimal tissue damage caused by the procedure. A factor that may play a role is the use of a tourniquet. A large majority of orthopaedic surgeons prefer to operate within a 'dry field', which is obtained by the use of a tourniquet. Tourniquet applied surgery is not without risks. Although its use during orthopedic surgery is widely accepted and a standard procedure, tourniquet use can lead to loss of muscle functional strength and contractile speed, vessel wall damage and nerve injury, next to the possibly increased risk of venous thrombosis. In the proposed study the investigators will investigate the effect of a tourniquet on local and systemic markers of hypoxia, inflammation, involvement of endothelium, and coagulation activation. A finding of more prominent activation of the coagulation system with tourniquet use than with non-use will create an important opportunity to prevent thromboembolic events in these patients, as it has been shown that knee arthroscopy can be performed adequately without the use of a tourniquet. Furthermore, it will increase the understanding of the pathophysiology of thrombosis.

NCT ID: NCT02555111 Completed - Clinical trials for Deep Vein Thrombosis

Xarelto Versus no Treatment for the Prevention of Recurrent Thrombosis in Patients With Chronic Portal Vein Thrombosis.

RIPORT
Start date: September 2015
Phase: Phase 3
Study type: Interventional

Open randomized therapeutic study to assess the efficacy of Xarelto 15mg/day in the recurrence of thromboembolic event compared to an untreated group in patients with chronic portal vein thrombosis without high risk thrombophilia.

NCT ID: NCT02553720 Completed - Venous Reflux Clinical Trials

The ATLANTIS Trial

ATLANTIS
Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether addition of aquatic exercise to conventional treatment helps reduce the adverse outcomes of chronic venous insufficiency including CVI resulting from venous thrombosis.

NCT ID: NCT02552420 Completed - Clinical trials for Deep Venous Thrombosis

The Clinical Application of Infrared Thermal Imaging Detecting Venous Thromboembolism

Start date: September 2007
Phase: Phase 2/Phase 3
Study type: Observational

The purpose of this study is to determine the effectiveness of infrared thermal imaging in adjunctive diagnostic screening for lower limb deep venous thrombosis (DVT).