Clinical Trials Logo

Venous Thrombosis clinical trials

View clinical trials related to Venous Thrombosis.

Filter by:

NCT ID: NCT02526303 Withdrawn - Liver Cirrhosis Clinical Trials

Anticoagulation for Non-occlusive Portal Vein Thrombosis in Patients With Liver Cirrhosis

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of anticoagulation in the treatment of non-occlusive portal vein thrombosis in patients with liver cirrhosis.

NCT ID: NCT02523937 Completed - Clinical trials for Deep Vein Thrombosis (DVT)

Evaluation of Soluble Fibrin in Thrombosis Exclusion

FSET
Start date: September 2015
Phase:
Study type: Observational

The purpose of the study is to evaluate the performances of Soluble Fibrin assay for exclusion of Pulmonary Embolism and Deep Venous Thrombosis. Secondary objectives are to determine the threshold value from the ROC curves, the possible interest in the positive diagnosis of Venous Thromboembolism (VTE), and to verify the absence of influence of age on the SF results.

NCT ID: NCT02507180 Recruiting - Pregnancy Clinical Trials

Safely Ruling Out Deep Vein Thrombosis in Pregnancy With the LEFt Clinical Decision Rule and D-Dimer

LEaD
Start date: September 2015
Phase:
Study type: Observational

This is prospective cohort study in pregnant women who present with signs and symptoms of possible deep vein thrombosis (DVT). All patients will have the same method of assessment of their DVT symptoms (the LEFt clinical decision rule will be applied and D-dimer test will be done) to determine if a compression ultrasound is required. All patients will be followed for a period of 3 months.

NCT ID: NCT02506985 Terminated - Pulmonary Embolism Clinical Trials

XENITH: Rivaroxaban for Pulmonary Embolism Managed With Catheter Directed Thrombolysis

XENITH
Start date: July 2015
Phase: Phase 4
Study type: Interventional

The trial is an open-label, randomized, trial examining novel biomarkers of thrombosis in patients managed with rivaroxaban vs. standard care following treatment of pulmonary embolism (PE) with catheter-guided alteplase. Patients >18 years old who present with PE and are managed with catheter-guided alteplase will be screened for study inclusion. Patient's meeting inclusion/exclusion criteria will undergo informed consent. Immediately following completion of alteplase infusion, patients will be randomized to receipt of rivaroxaban 15 mg oral bid for 21 days followed by 20mg oral daily or continuation on unfractioned heparin or low-molecular weight heparin with initiation of warfarin adjusted to INR of 2-3. Blood samples will be taken within 2 hours of CDT completion prior to receipt of study treatment (study day 1), at 8h-12h, 24h, 48h, 5d (or prior to hospital discharge), and at 30 day follow-up. Clinical endpoints, including bleeding, evidence of thrombosis progression, and death will be tracked during index hospitalization and at follow-up 30 days post-discharge.

NCT ID: NCT02502396 Completed - Cancer Clinical Trials

Rivaroxaban Utilization for Treatment and Prevention of Thromboembolism in Cancer Patients: Experience at a Comprehensive Cancer Center

Start date: September 28, 2015
Phase:
Study type: Observational

The primary objective of this study is to evaluate the practice patterns of rivaroxaban usage invenous-thromboembolism (VTE) and non-valvular atrial fibrillation (NVAF) in cancer patients. The secondary objectives are to evaluate outcomes such as recurrent VTE, stroke and bleeding for cancer patients on rivaroxaban.

NCT ID: NCT02489721 Completed - Clinical trials for Upper Extremity Deep Vein Thrombosis

Major Complications Related to PICC and Midline Insertion

PICC/MIDLINE
Start date: June 2015
Phase:
Study type: Observational [Patient Registry]

Most important peripherally inserted central catheter (PICC) and Midline complications are thrombosis and catheter related blood stream infections. No large prospective observational study are present in literature about these topics. The aim of this multicenter prospective observational study is to analyze all the complications due to PICC and Midline insertion.

NCT ID: NCT02486445 Completed - Clinical trials for Deep Venous Thrombosis

Rivaroxaban for Scheduled Work-up of DVT - The Ri-Schedule Study

Ri-Schedule
Start date: March 2015
Phase: Phase 3
Study type: Interventional

This prospective outcome study is designed to assess the safety of rivaroxaban in the pre-diagnosis phase of DVT.

NCT ID: NCT02485184 Recruiting - Liver Cirrhosis Clinical Trials

TIPS vs Endoscopic Therapy for Variceal Rebleeding in Cirrhotic Patients With Portal Vein Thrombosis

Start date: July 9, 2017
Phase: N/A
Study type: Interventional

portal vein thrombosis may be a negative prognostic marker of variceal bleeding in liver cirrhosis. Compared with conventional endoscopic and pharmacological therapy, transjugular intrahepatic portosystemic shunt may further improve the outcomes of portal vein thrombosis in liver cirrhosis with variceal bleeding.

NCT ID: NCT02480790 Active, not recruiting - Ovarian Cancer Clinical Trials

Venous Thromboembolic Complications in Ovarian Cancer

Start date: November 2014
Phase:
Study type: Observational

Objectives of the study are: To estimate the incidence of venous thromboembolism (VTE) in a cohort of women with suspected ovarian cancer and evaluate changes in the coagulation system in case of benign or malignant disease. The impact of changes in the coagulation system on disease prognosis will be evaluated.

NCT ID: NCT02469376 Terminated - Clinical trials for Deep Vein Thrombosis

Evaluation of a New Imagingtechnologie for Thrombosis

PET-GP1_1
Start date: September 2014
Phase: Phase 1
Study type: Interventional

Arterial and venous thrombi play an important role in various vascular diseases such as myocardial infarction, stroke, transient ischemic attacks (TIA) and pulmonary embolism. These thromboembolic disorders are the leading causes of morbidity and mortality worldwide. A non-invasive method for the quantitative and effective detection of thrombi in the whole body has not yet been established. In spite of the available techniques, 30% to 40% of ischemic strokes "cryptogenic" (undetermined cause, the source of thromboembolism is never identified). Possible causes of cryptogenic stroke atherosclerosis include in the aortic arch or intracranial arteries. A plaque in the arch or other large vessels could be an important source of cryptogenic strokes, however, are those difficult to detect by routine methods. The approach of thrombus targeted molecular imaging could identify potentially troublesome plaques early on before they become a dangerous rupture. The hypothesis is that the radiotracer 18F-arterial GP1 and venous thrombi using positron emission tomography (PET) can be made visible. The primary goal is the potential applicability of the substance as a PET tracer for diagnosing thrombi.