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Peripheral Vascular Disease clinical trials

View clinical trials related to Peripheral Vascular Disease.

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NCT ID: NCT02834221 Completed - Atrial Fibrillation Clinical Trials

Ultrasound-guided Femoral Vein Accessibility, Safety and Time for Atrial Fibrillation Treatment

ULTRA-FAST
Start date: June 2016
Phase: N/A
Study type: Interventional

This study is designed to evaluate the use of real-time ultrasound-guided femoral venipuncture during pulmonary vein isolation for treating atrial fibrillation .

NCT ID: NCT02831075 Recruiting - Diabetic Foot Clinical Trials

A Clinical Study Using Adipose-derived Stem Cells for Diabetic Foot

Start date: January 2015
Phase: Phase 1
Study type: Interventional

Stem cell therapy has been a new and effective therapy in recent years for diabetic foot.This study intends to establish an optimal clinical research program, and attempts to break the technical bottleneck in the stem cell therapy for treating diabetes related vascular complications.

NCT ID: NCT02823444 Completed - Clinical trials for Peripheral Arterial Disease

Non-Contrast Enhanced Peripheral Magnetic Resonance Angiography

Start date: April 2008
Phase:
Study type: Observational

To systematically develop, test, and refine peripheral vascular electrocardiography-gated fast spin echo magnetic resonance imaging for the accurate diagnosis of peripheral arterial disease without gadolinium contrast. To test prospectively the accuracy of fast spin echo in peripheral arterial disease patients, compared with bolus-chase and time-resolved gadolinium enhanced magnetic resonance angiography. Additionally, as a substudy of this project, we will compare our fast spin echo approach with alternative non-contrast-enhanced magnetic resonance imaging methods such as time-of-flight and steady-state gradient echo imaging. The overarching goals of our research are to develop and validate a peripheral magnetic resonance imaging technique that accurately depicts anatomy and disease without exposing patients to exogenous contrast material and its associated risks.

NCT ID: NCT02805023 Recruiting - Clinical trials for Peripheral Arterial Disease

BGC101 (EnEPC) Autologous Cell Therapy From Patient's Own Blood for Treatment of Critical Limb Ischemia (CLI)

EnEPC-CLI
Start date: June 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Evaluate the feasibility of an autologous cell preparation composed of a mixture of cells enriched for endothelial progenitor cells (EnEPCs) and multipotent adult hematopoietic stem/progenitor cells (HSPC) (BGC101), in the treatment of patients suffering from peripheral arterial disease (PAD) with critical limb ischemia (CLI) who have not responded to optimal pharmacological treatment or control of risk factors and/or had a revascularization failure, and do not have the option of further revascularization treatment.

NCT ID: NCT02796079 Recruiting - Diabetic Foot Clinical Trials

A Clinical Study Using Autologous Bone Marrow Stem Cell for Diabetes Related Vascular Complications

Start date: January 2015
Phase: Phase 1
Study type: Interventional

Stem cell therapy has been a new and effective therapy in recent years for diabetic foot.This study intends to establish an optimal clinical research program, and attempts to break the technical bottleneck in the stem cell therapy for treating diabetes related vascular complications.

NCT ID: NCT02786173 Completed - Clinical trials for Peripheral Arterial Disease

Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry"

PRIME
Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

The PRIME Registry is a multi-center, observational study designed to evaluate immediate and long-term outcomes (36 months) of endovascular revascularization in patients with critical limb ischemia (CLI) and advanced peripheral artery disease (PAD).

NCT ID: NCT02767895 Terminated - Clinical trials for Peripheral Artery Disease

Prehabilitation for PAD Revascularization Patients

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Patients undergoing elective revascularization of their peripheral artery disease will be randomized to a prehabilitation program or usual care prior to their scheduled procedure.

NCT ID: NCT02767011 Completed - Clinical trials for Peripheral Vascular Disease

Tele-Health Electronic Monitoring to Reduce Post Discharge Complications and Surgical Site Infections

THEM
Start date: July 2016
Phase: N/A
Study type: Interventional

Abstract: It is intuitive that post discharge surgical complications are associated with increased patient dissatisfaction, and directly associated with an increase in medical expenditures. It is also easy to make the connection that many post hospital discharge surgical complications including surgical site infections could be influenced or exacerbated by patient co-morbidities. The authors of a recent study reported that female gender, obesity, diabetes, smoking, hypertension, coronary artery disease, critical limb ischemia, chronic obstructive pulmonary disease, dyspnea, and neurologic disease were all of among significant predictors of surgical site infections after vascular reconstruction was performed. The main concern for optimal patient care especially in geographically isolated areas of West Virginia is to have early, expeditious, and prompt diagnosis of early surgical site infection with subsequent indicated interventions. This theme will lead to patient satisfaction, minimizing third party interventions and decrease the total cost associated with these complications. Nevertheless, it seems reasonable to believe that monitoring using telehealth technology and managing the general health care patients receive after a hospital vascular intervention will improve overall health and reduce post-operative complications. Aims/Objectives: 1. The primary objective of the current project is to compare early and late outcomes for patients who receive post discharge health care monitoring (which includes using Telehealth electronic monitoring; THEM) to patients who receive standard of care (SOC) and routine discharge instructions and no monitoring. Methods: 1. Randomize patients who are scheduled to have revascularization interventions with groin incisions to receive either telehealth electronic health care monitoring or normal standard of follow-up care. 2. Follow patients for 4 weeks, record any 30-day hospital readmissions or complications. In addition, have participants complete the follow-up survey questionnaires.

NCT ID: NCT02734095 Not yet recruiting - Clinical trials for Peripheral Vascular Disease

Determining Predictors of Restenosis in Femoropopliteal Lesions

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

A prospective, single-center, real-world study on intravascular ultrasound measurements after percutaneous transluminal angioplasty and stenting in the treatment of femoropopliteal lesions.

NCT ID: NCT02685098 Active, not recruiting - Clinical trials for Cardiovascular Disease

A Clinical and Histological Analysis of Mesenchymal Stem Cells in Amputation

CHAMP
Start date: January 23, 2017
Phase: Phase 1
Study type: Interventional

Patients undergoing semi-elective lower extremity major amputation from complications associated with atherosclerotic limb ischemia will received intra-muscular injections of allogeneic Mesenchymal Stromal Cells in the leg above and below the point of amputation to prevent ischemic wound complications after surgery and decrease the incidence of revision and further amputation. Cohort Groups 1-4 will serve as controls.