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Deep Venous Thrombosis clinical trials

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NCT ID: NCT01221805 Completed - Pulmonary Embolism Clinical Trials

STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism

DiET
Start date: November 2011
Phase: Phase 4
Study type: Observational

The purpose of this study is to demonstrate the ability of STA® Liatest® D-Di combined with a clinical pretest probability (PTP) to safely exclude pulmonary embolism (PE) or Deep Venous Thrombosis (DVT) in a 3 month follow-up.

NCT ID: NCT01140386 Completed - Clinical trials for Venous Thromboembolism

Prevalence and Risk Factors of Venous Thromboembolism in Hospitalized Pediatric Patients

pediatric DVT
Start date: May 2009
Phase: N/A
Study type: Observational

The issue to be studied is the prevalence of venous thromboembolism (VTE) in hospitalized pediatric patients, and to identify if there are subgroups of patients who may be at higher risk. There are two hypotheses that will be looked at in this study. The first hypothesis is that individual risk factors for VTE in hospitalized pediatric patients are: age >14, obesity, black race, female sex, presence of a central venous line (CVL), traumatic mechanism of injury, orthopaedic surgery, and use of oral contraceptives. The second hypothesis is that risk factors have an additive effect such that risk stratification can be developed to identify those patients with the highest risk.

NCT ID: NCT01104337 Completed - Stroke Clinical Trials

Drug Interaction Between Paracetamol and Warfarin

INPAWA2
Start date: March 2007
Phase: Phase 4
Study type: Interventional

The objective of this study is to investigate whether paracetamol, given at therapeutic doses (2g/day and 3 g/day), may potentiate the anticoagulant effect of warfarin.

NCT ID: NCT00894283 Completed - Pulmonary Embolism Clinical Trials

Comparing Enoxaparin to Fondaparinux to Prevent Venous Thromboembolism (VTE) in Bariatric Surgical Patients

Start date: June 2009
Phase: Early Phase 1
Study type: Interventional

This pilot study is designed to determine the feasibility of conducting a randomized clinical trial comparing fondaparinux sodium (Arixtra) once daily with enoxaparin (Lovenox®) twice daily with respect to preventing deep vein thrombosis (DVT) and pulmonary embolism (PE) after bariatric surgery in obese patients.

NCT ID: NCT00812370 Completed - Clinical trials for Deep Venous Thrombosis

The UNBLOCK Study: Utilization of Bivalirudin On Clots in Kids

UNBLOCK
Start date: September 2008
Phase: Phase 1
Study type: Interventional

Thrombosis is a significant medical complication in children with chronic diseases. The currently utilized treatments have many drawbacks which can lead to poor outcomes. More modern therapies are available but have not been systematically tested in children. This study will determine whether one such medication, bivalirudin is a safer and more effective alterative. This study will monitor what effects the drug has upon the child's body and how the body processes the study drug (absorption, metabolism and elimination). The study will also evaluate the drug's effectiveness by following how long it takes to dissolve the clot. The safety issues being monitored relate to any observations of major or minor bleeding episodes after taking the drug, and/or any other side effects.

NCT ID: NCT00660205 Completed - Gastric Cancer Clinical Trials

Venous Thromboembolism and Haemostatic Disturbances in Patients With Upper Gastrointestinal Cancer

GIVTE
Start date: February 2008
Phase: N/A
Study type: Observational

Cancer is a well known risk factor for venous thromboembolism (VTE) such as deep venous thrombosis (DVT) and pulmonary embolism (PE). Today we know that patients with adenocarcinomas of the gastro intestinal tract (GI-tract) often is in a hypercoagulable state. In our observational study we collect patients admitted to department with a tentative diagnosis of upper GI cancer including pancreas cancer and offer them flow doppler ultrasounds of both legs for diagnosis of DVT in the entire treatment time. The routine CT-scan of the chest is modified to diagnose PE. This will be compared with blood samples analysed for coagulation markers including D-dimer - a fibrinogen degradation product.

NCT ID: NCT00628576 Completed - Clinical trials for Deep Venous Thrombosis

Evaluation of Long-Term Sequelae After Thrombophlebitis, i.e. Deep Venous Thrombosis of the Lower Extremities

Start date: October 1993
Phase: Phase 3
Study type: Interventional

The purpose of the study was to evaluate efficacy and safety of the new acute treatment of deep venous thrombosis by use of low-molecular-weight heparin compared with standard treatment using unfractionated heparin, especially concerning long-term morbidity.

NCT ID: NCT00622102 Completed - Atrial Fibrillation Clinical Trials

Testing Strategies to Improving Warfarin Adherence

Start date: December 2007
Phase: N/A
Study type: Interventional

We are performing a research study to learn more about the control of an individual's blood thinning (anticoagulation) on warfarin. Individuals from an anticoagulation clinic are being asked to participate in order to see if a lottery which provides the opportunity to win money in combination with the use of the Med-eMonitor might be useful in helping patients to achieve better control of their anticoagulation therapy. Half of the participants will be enrolled in the lottery arm and the other half will be a control group who will receive the Med-eMonitor only.

NCT ID: NCT00603317 Completed - Atrial Fibrillation Clinical Trials

Pharmacodynamic Drug Interaction Between Warfarin and Amoxicillin-clavulanic Acid

INWARA
Start date: March 2008
Phase: Phase 4
Study type: Interventional

Several case reports indicate that the use of the antibiotic combination amoxicillin and clavulanic acid (AM-CLAVAC) can interact with warfarin pharmacodynamics. However, fever per se might also be responsible of these warfarin overdose reports, as well as the use of high dose paracetamol. The aim of the present study is to determine if AM-CLAVAC can increase the pharmacodynamics of warfarin among patients at steady state Double blinded cross over controlled study vs placebo performed in 12 evaluable patients treated with warfarin with an INR target 2 to 3 and a stable INR and a stable dose.

NCT ID: NCT00329433 Completed - Clinical trials for Deep Venous Thrombosis

Study Comparing Desirudin With Heparin to Prevent Vein Clots After Heart and Lung Surgery

Start date: May 2006
Phase: Phase 2/Phase 3
Study type: Interventional

A blood clot in the veins, also known as deep venous thrombosis (DVT), is one of the most common complications after surgery. This may result in death if a clot breaks off and travel to the lungs; this is referred to as pulmonary embolism (PE). After heart surgery the incidence of DVT ranges from 20-48% and following lung surgery the incidence is 19-26%. In order to decrease the likelihood of this complication, patients receive by injection a blood thinning medicine. Heparin is the usual medicine used for this purpose following heart and lung surgery. Recently there have been reports that other medicines may be more effective than heparin for this purpose. Also there have been reports that some patients develop antibodies to heparin. When this occurs, this may prevent the heparin from being effective and may even promote the formation of blood clots. Antibodies to heparin may be present more often following heart and lung surgery than other types of surgery. There is a new medicine called desirudin (Iprivask), which may be used instead of heparin to prevent blood clots following heart and lung surgery. Desirudin is currently approved by the FDA to prevent blood clots following hip surgery. The purpose of this study is to compare desirudin with heparin for the prevention of vein clots after heart and lung surgery.