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Thrombosis clinical trials

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NCT ID: NCT01086046 Recruiting - Thrombosis Clinical Trials

Study of Blood Clotting After Transcatheter Atrial Septal Defect Closure

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate blood clots after Percutaneous ASD Closure in different age, sexuality and defective diameter; evaluating the relationship of blood clotting with Occluder, injury of intima and inflammation;comparation of the effect and safety between different anticoagulation after Percutaneous ASD Repair; explore propose an optimal anticoagulation plan.

NCT ID: NCT01063426 Recruiting - Surgery Clinical Trials

Re-STOP DVT: Reload of High Dose Atorvastatin for Preventing Deep Vein Thrombosis in Statin Users

Re-STOP DVT
Start date: November 2009
Phase: Phase 4
Study type: Interventional

Reload of high dose statin may have potential for preventing deep vein thrombosis (DVT) in patients on statin undergoing total knee replacement arthroplasty. A body of evidence have been reported that reloading of atorvastatin have efficacy in reducing periprocedural myocardial infarction and contrast induced nephropathy. These effects are considered to be mainly due to their antioxidant anti-thrombotic and anti-inflammatory property. We, therefore, hypothesize that high dose atorvastatin re-loading may prevent DVT.

NCT ID: NCT01046942 Recruiting - Thrombosis Clinical Trials

ThrombElastoGraphic Haemostatic Status and Antiplatelet Therapy After Coronary Artery Bypass Graft Surgery

TEG-CABG
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether adding clopidogrel to aspirin after coronary bypass operation (CABG) improves graft patency, in patients that have preoperatively increased platelet activity(hypercoagulable) and therefore greater risk of graft occlusion( thrombosis).

NCT ID: NCT01029821 Recruiting - Clinical trials for Deep Venous Thrombosis

Low-Molecular-Weight Heparin (LMWH) for Deep Venous Thrombosis (DVT) Prophylaxis

Start date: February 2010
Phase: N/A
Study type: Interventional

1. The use of LMWH following open reduction and internal fixation of ankle fractures will reduce the number of thrombi formed. 2. The rates of clinically significant DVT will be equivalent between two groups.

NCT ID: NCT01021488 Recruiting - Thrombosis Clinical Trials

Rosuvastatin for Preventing Deep Vein Thrombosis

STOP-DVT
Start date: October 2009
Phase: Phase 4
Study type: Interventional

Deep vein thrombosis (DVT)is devastating disease which influencing the mortality and morbidity of patients at-risk like those undergoing orthopedic surgery. Recent publication suggested HMO-co-A reductase inhibitor (statin) may reduce the occurrence rate of venous thromboembolism in apparently healthy persons. The pleiotropic property of statin like antioxidant, antithrombotic, anti-inflammatory may have effect on the positive results. We are investigating whether rosuvastatin is associated with lower incidence of deep vein thrombosis (DVT) in patients undergoing total knee replacement arthroplasty(TKRA)who are at-high risk for developing DVT

NCT ID: NCT00733434 Recruiting - Thrombosis Clinical Trials

The Use of Prostaglandin E1 in Head and Neck Microsurgery

PGE1HNM
Start date: July 2008
Phase: Phase 4
Study type: Interventional

Prostaglandin E1 (PGE1 )has been shown to have vasodilatation and anti-thrombosis effects, so it is used by some surgeons after microsurgery to keep the patency of the anastomosed small vessels. However, PGE 1 may also causes some complications, like pleural effusion or deep vein thrombosis. Therefore, it remains uncertain whether a routine use of PGE 1 after head and neck microsurgery is justified. We aim to test the hypothesis that PGE 1 increases postoperative vessel patency rate in patients undergoing head and neck microsurgery, with a comparable complication rate as the control group.

NCT ID: NCT00714909 Recruiting - Breast Cancer Clinical Trials

Determination of Predictive Value of Echography Doppler Abnormalities

CAVECCAS
Start date: November 2008
Phase: N/A
Study type: Observational

In order to avoid to use a traumatic and iatrogenic examen (phlebography), the purpose of the study is to validate echography doppler in the diagnosis of asymptomatic related catheter related thrombosis.

NCT ID: NCT00677846 Recruiting - Clinical trials for Deep Venous Thrombosis

Venous Thrombus Investigation With Contrast Enhanced Ultrasound Imaging

Start date: April 2007
Phase: N/A
Study type: Observational

Background: During the repair process of deep venous thrombosis, capillary formation is seen from day 18 to day 25. Contrast agent investigation is well known to detect small vessels in arterial disease. We intend to use this method to detect early vascularisation in the thrombus, in order to get more information about the evolution of the thrombosis in vivo. Aims of the study: Investigation of a newly diagnosed occluding venous thrombus with duplexsonography, using contrast agent and compare the degree of vascularization in the same patient after 3 weeks and 3 months. The relative signal intensity difference (baseline to peak) of the time intensity curve (TIC) is measured in defined region of interests (ROI). Comparison of the visibility of revascularisation between color duplexsonography, power mode and contrast agent will be done. Method: Patients with venous thrombosis of the proximal limb veins (femoral or popliteal vein) will be investigated with ultrasound agent in supine position. 5 ml of the contrast agent sulfur hexafluoride is given intravenously into a vein of the dorsal foot. The measurements are done in a defined area, where the thrombus is fully occluding in color Doppler investigation. The regions of interest will be the vessel walls and the centre of the thrombus in cross section view. The signal intensities are measured at baseline and peak (in decibel) in the centre and in the peripheral part of the vein. 20 patients with acute deep venous thrombosis will be included in this pilot study and investigated at baseline, after 3 weeks and 3 months. Previously (before contrast agent application), the veins are investigated with color - and power Doppler to test visibility in comparison to the contrast agent investigation.

NCT ID: NCT00653601 Recruiting - Bleeding Clinical Trials

Bridging Therapy in Patients at High Risk for Stent Thrombosis Undergoing Surgery

Start date: April 2008
Phase: N/A
Study type: Observational

Patients who have undergone placement of coronary stents require dual antiplatelet therapy with Plavix and aspirin to prevent the serious complication of in-stent thrombosis. Some of these patients will require surgery while on dual antiplatelet therapy. This poses a challenge because being on Plavix is associated with higher risks of perioperative bleeding, but stopping Plavix puts patients at increased risk for in-stent thrombosis. Currently, the ACC/AHA guidelines recommend discontinuation of Plavix five days prior to surgery to prevent bleeding complications. However, there are no universal recommendations for preventing in-stent thrombosis. Some experts recommend the use glycoprotein IIb/IIIa inhibitors (short-acting antiplatelet agents) as "bridging therapy" during the high-risk perioperative period. Although these agents should be beneficial based on theory, there is currently no published data on their effectiveness for this purpose. The current study proposes to evaluate the value of Aggrastat (a short-acting intravenous platelet glycoprotein IIb/IIIa inhibitor) in decreasing the risk of in-stent thrombosis without increasing the risk of perioperative bleeding.

NCT ID: NCT00517257 Recruiting - Thrombosis Clinical Trials

Atorvastatin for the Treatment of Retinal Vein Occlusion

ATORVO
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The ATORVO study is designed to determine whether atorvastatin (Lipitor) can improve vision, when compared to placebo