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Thromboembolism clinical trials

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NCT ID: NCT00662688 Terminated - Pancreatic Cancer Clinical Trials

Chemotherapy With or Without Dalteparin in Treating Patients With Metastatic Pancreatic Cancer

PAM07
Start date: October 2007
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Anticoagulants, such as dalteparin, may help prevent blood clots from forming in patients being treated with chemotherapy. It is not yet known whether gemcitabine is more effective when given alone or together with dalteparin and/or capecitabine in treating patients with pancreatic cancer. PURPOSE: This randomized phase III trial is studying whether dalteparin prevents blood clots in patients with pancreatic cancer receiving treatment with different combinations of gemcitabine and capecitabine.

NCT ID: NCT00655122 Terminated - Clinical trials for Deep Vein Thrombosis

Prophylaxis In Venous Thromboembolism In Primary Care, A Pilot Study

Start date: April 2003
Phase: Phase 4
Study type: Interventional

The primary objective was to study the clinical benefit with dalteparin sodium in thromboprophylaxis in primary care medical subjects. The secondary objective was a pharmacoeconomic evaluation of hromboprophylaxis with dalteparin sodium in primary care medical subjects.

NCT ID: NCT00580216 Terminated - Atrial Fibrillation Clinical Trials

Evaluation of Weekly Subcutaneous Biotinylated Idraparinux Versus Oral Adjusted-dose Warfarin to Prevent Stroke and Systemic Thromboembolic Events in Patients With Atrial Fibrillation

BOREALIS-AF
Start date: December 2007
Phase: Phase 3
Study type: Interventional

The objective is to evaluate whether once weekly subcutaneous (SC) injection of idrabiotaparinux is at least as efficient to prevent clots in brain and in the other organs than oral international normalized ratio (INR) adjusted-dose warfarin in patients with atrial fibrillation (AF).

NCT ID: NCT00493896 Terminated - Clinical trials for Venous Thromboembolism

Safety of Fondaparinux as Routine VTE Prophylaxis in Medical ICU Patients

Start date: July 2007
Phase: Phase 3
Study type: Interventional

This is a pilot study to evaluate safety of fondaparinux and enoxaparin in terms of bleeding and development of thrombocytopenia in the medical ICU population.

NCT ID: NCT00445328 Terminated - Clinical trials for Venous Thromboembolism

Dalteparin vs Unfractionated Heparin For The Prevention Of Venous Thromboembolism (VTE) In Hospitalized Acutely Ill Medical Patients

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of dalteparin vs unfractionated heparin for the prevention of VTE (Venous Thromboembolism) in hospitalized acutely ill medical patients.

NCT ID: NCT00437892 Terminated - Clinical trials for Hypercholesterolemia

Statins to Reduce D-dimer Levels in Patients With Venous Thrombosis

Start date: May 2007
Phase: Phase 2
Study type: Interventional

Elevated levels of D-dimer, a marker of procoagulant state, have been identified as a marker of an increased risk of recurrent VTE. Statins have proven antithrombotic properties, as suggested by the reduction of several prothrombotic markers, including D-dimer, in patients at high risk of arterial thrombosis. Such antithrombotic properties could also be observed in patients at high risk of venous thrombosis. Aim of the study is to assess the effect of statins on D-dimer levels in patients with previous VTE after oral anticoagulant treatment withdrawal.

NCT ID: NCT00437697 Terminated - Clinical trials for Venous Thromboembolism

Thromboprophylaxis in Critically Ill Patients

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Intensive care patients are at high risk to develop deep venous thrombosis and pulmonary embolism. Despite anticoagulation with heparin 7% of ICU patients suffer from this serious complication. Optimal regimens for prevention of VTE have been established in medical patients only and are not known for ICU patients. It was therefore the aim of this study to compare the bioavailability of a low molecular weight heparin in ICU patients and in medical patients. Furthermore, we looked wether a 50% dose increase resulted in better bioavailability of this drug.

NCT ID: NCT00428441 Terminated - Clinical trials for Venous Thromboembolism

D-dimer to Predict Recurrence in Patients With Multiple Episodes of Venous Thromboembolism

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

Optimal duration of oral anticoagulant therapy in patients with recurrent episodes of venous thromboembolism (VTE) is a matter of debate and recommendations are based on inadequate evidence. More than 12 months of treatment are currently recommended, and the grade of recommendation is low. The PROLONG study has recently evaluated the predictive role of D-dimer measurement after withholding oral anticoagulant treatment in patients with a first episode of VTE. Patients with a positive D-dimer had a significantly higher incidence of VTE recurrences than patients with a negative D-dimer and required resumption of the antithrombotic treatment. Based on the results of this and of previous cohort studies, it appears safe to withhold treatment in patients with negative D-dimer values and to continue treatment in patients with altered D-dimer levels. Aim of this study is therefore to assess the negative predictive value of D-dimer also in patients with recurrent VTE and to evaluate the clinical utility of this approach in this patient setting.

NCT ID: NCT00423683 Terminated - Cancer Clinical Trials

Anticoagulation and Inferior Vena Cava Filters in Cancer Patients With a Venous Thromboembolism

Start date: January 2007
Phase: Phase 3
Study type: Interventional

The development of clots is a potentially deadly complication in many cancer patients. The current optimal treatment is unknown. Evidence supporting the effectiveness of the use of Inferior Vena Caval Filters is lacking. This study will compare the two standard of care treatment options: anticoagulation with or without a inferior vena cava filter. The anticoagulation medication chosen will be Arixtra and it will be given once a day as an injection. Patients will be called at various intervals to monitor their signs and symptoms of new thromboembolisms.

NCT ID: NCT00303407 Terminated - Cancer Clinical Trials

Prophylaxis of Venous Thrombo-Embolism in Cancer Patients Under Palliative Care

Start date: January 2001
Phase: Phase 4
Study type: Observational

To determine the efficacy and to measure the complications of prophylactic anticoagulation using low-molecular weight heparin in adult cancer patients under palliative care