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Deep Venous Thrombosis clinical trials

View clinical trials related to Deep Venous Thrombosis.

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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).

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: NCT02411292 Completed - Clinical trials for Venous Thromboembolism

Enoxaparin Metabolism in Reconstructive Surgery Patients

Start date: March 2015
Phase: Phase 2
Study type: Interventional

Venous thromboembolism (VTE) is a leading cause of death among hospitalized patients, and is an important patient safety issue in plastic surgery. Previous work has shown that enoxaparin prophylaxis can prevent many post-operative VTE events, and current American Society of Plastic Surgeons guidelines support enoxaparin prophylaxis for high-risk patients. Highest risk patients often have cancer or trauma reconstruction. Primary outcomes include 1) peak and trough steady-state aFXa levels in response to standard and escalated doses of enoxaparin and 2) the proportion of patients with appropriate aFXa levels pre and post initiation of a clinical protocol for enoxaparin dose adjustment. The investigators expect that standard dosing will result in inadequate aFXa peak and trough levels, and that the clinical dose adjustment protocol will significantly improve the proportion of in-range aFXa levels. The investigators will also develop a linear regression-based equation to calculate, based on patient-level factors, the required dose of enoxaparin to generate in-range aFXa levels. This research may show that the current "one size fits all" approach to enoxaparin prophylaxis is insufficient. In the trauma and orthopaedic populations, patients with low initial aFXa levels are significantly more likely to develop deep venous thrombosis. Thus, this study has important implications for appropriate enoxaparin dose magnitude and frequency, and may ultimately help to decrease the substantial morbidity and mortality associated with post-operative VTE.

NCT ID: NCT02402881 Completed - Pulmonary Embolism Clinical Trials

Education Bundle to Decrease Patient Refusal of VTE Prophylaxis

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

The investigators have recently developed a registry of missed doses of VTE prophylaxis that includes retrospective data on missed doses of VTE prophylaxis. To decrease rates of VTE prophylaxis refusal, the group has developed a patient-centered education bundle that will be delivered as an in-person, 1-on-1 discussion session with a nurse educator. Supporting education materials include a 2-page education sheet and an educational video. The investigators hypothesize that patient refusal of VTE prophylaxis is associated with significant knowledge gaps among patients regarding patients' risk of developing VTE and the benefits of VTE prophylaxis and that delivering an education bundle to patients that refuse VTE prophylaxis will improve compliance with VTE prophylaxis and decrease rates of VTE.

NCT ID: NCT02376803 Completed - Atrial Fibrillation Clinical Trials

The Effect of Medication Timing on Anticoagulation Stability in Users of Warfarin: The "INRange" RCT

Start date: February 2015
Phase: Phase 4
Study type: Interventional

Warfarin is an anticoagulant medication that is highly effective at preventing clotting disorders but which has a narrow therapeutic window. If warfarin is under effective patients are at risk of stroke, if it is over effective patients are at risk of bleeding complications. Physicians routinely and regularly measure a blood test (called the "INR") that determines the effectiveness of warfarin and have a range of test values (the "therapeutic range") in which they try to keep the patient. By convention warfarin is taken at dinnertime, however this is the same time of day that highly variable consumption of dietary vitamin K occurs (found largely in green leafy vegetables) and vitamin K alters the effectiveness of warfarin. Given vitamin K has a very short half-life (i.e. it is only active for a short period of time after it is ingested) it may make more sense to take warfarin in the morning (when very little vitamin K is ingested) to produce a more consistent drug effect. The purpose of this study is to determine whether switching current warfarin users from evening to morning dosing decreases time spent outside the therapeutic INR range.

NCT ID: NCT02361294 Completed - Clinical trials for Deep Venous Thrombosis

Immature Plateletes in the Etiopathology of Deep Venous Thrombosis

iPLATELET
Start date: December 2014
Phase:
Study type: Observational

The study is designed to evaluate the role of platelets and immature platelets in the ethiopathology of deep venous thrombosis and pulmonary embolism.

NCT ID: NCT02318472 Active, not recruiting - Clinical trials for Deep Venous Thrombosis

Early Mobilization After Achilles Tendon Rupture

EarlyM-Achil
Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether early mobilization after Achilles tendon rupture can speed up healing, prevent development of venous thromboembolism and improve patient outcome.

NCT ID: NCT02265523 Completed - Osteoarthritis Clinical Trials

Exercise and Cycle Ergometry Post TKA - A Randomized Controlled Trial

Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this investigation is to examine the effect of, and improve patient compliance and motivation following total knee arthroplasty; to determine the efficacy of two post-surgical exercise programs on knee pain, function, range of motion, strength, and swelling (girth); and to establish a panel of biomarkers that will allow: a) early identification of patients at risk (i.e. unable to complete post-operative treatment) and; b) predict the likelihood of a successful treatment outcome post-surgically.

NCT ID: NCT02211326 Completed - Atrial Fibrillation Clinical Trials

Genotype-guided Warfarin Individualized Treatment

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

The purpose of this study is to determine whether the international pharmacogenetic algorithm is better than the standard initiation dosing and whether the two algorithms are suitable for Chinese elderly patients.

NCT ID: NCT02123550 Recruiting - Clinical trials for Deep Venous Thrombosis

Doppler Ultrasound Imaging of Plastic Surgery Patients for DVT Detection

Start date: January 2014
Phase:
Study type: Observational

This prospective controlled study examines the use of Doppler ultrasound as a means to screen elective plastic surgery patients for the presence of deep venous blood clots both before and after surgery. This is a noninvasive technique that is known to be both sensitive and specific for the detection of deep venous thromboses in the lower extremities. This method may make it unnecessary to select patients for prophylactic anticoagulation, which poses additional risks to the patient.