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Peripheral Arterial Disease clinical trials

View clinical trials related to Peripheral Arterial Disease.

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NCT ID: NCT02369692 Terminated - Clinical trials for Peripheral Vascular Disease

Embolization Procedures in the Peripheral Vasculature Using the Magellan™ Robotic System

Start date: April 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this prospective study is to gather procedural use and safety data on the initial use of the Magellan Robotic System with the Magellan Robotic Catheter 6 Fr, Vascular Accessories 6 Fr and Microcatheter Driver This study will focus on, but not be limited to, endovascular embolization procedures in the peripheral vascular, for example, embolization of the splenic and hepatic arteries, uterine arterial embolization (UAE), prostatic arterial embolization (PAE), and trans-arterial chemoembolization (TACE). The data will be analyzed for medical education, societal presentation and/or publication by the investigator.

NCT ID: NCT02363894 Completed - Clinical trials for Peripheral Arterial Disease

DEFINITIVE AR Two Year Follow-up Extension Study

Start date: March 2015
Phase: N/A
Study type: Observational

The purpose of this DEFINITIVE AR Two Year Follow-up Extension Study is to gather data to assess and estimate the long term effect of treating a vessel with plaque excision (PE) in combination with paclitaxel-coated balloon angioplasty (PTX PTA) compared to treatment with PTX PTA alone.

NCT ID: NCT02341664 Completed - Stroke Clinical Trials

Patient and Provider Assessment of Lipid Management Registry

PALM
Start date: May 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of the Patient and Provider Assessment of Lipid Management Registry (PALM) is to gain a better understanding of physicians' cholesterol medication prescribing practices, patient and physician attitudes and beliefs related to cholesterol management, and current utilization of cholesterol-lowering therapies given the new ACC/AHA guideline recommendations. The PALM Registry hopes to allow for the design of ways to improve cholesterol management and decrease the burden of cardiovascular disease (CVD) in the US.

NCT ID: NCT02325466 Completed - Type 2 Diabetes Clinical Trials

Comparative Efficacy of Ticagrelor Versus Aspirin on Blood Viscosity in Peripheral Artery Disease Patients With Type 2 Diabetes

Start date: April 2015
Phase: Phase 3
Study type: Interventional

The hypothesis being that both aspirin-ticagrelor and ticagrelor monotherapy will be superior to aspirin monotherapy in the reduction of whole blood viscosity at the end of each 4 week treatment period. Study participants will be randomized into 3 groups, and each group will receive each of 3 treatments in the cross-over study. At the end of each individual 4 week treatment period the investigators will determine whether there are differences in low and high shear rate dependent viscosity and investigate the effect of the treatment on peripheral arterial blood flow using pulse volume recordings, ankle brachial index and toe pressures. Subjects will be eligible if they have ankle-brachial index less than or equal to 0.85, or if a patient's blood vessels are calcified, patients will have toe-brachial index less than or equal to 0.6 performed using continuous-wave Doppler.

NCT ID: NCT02317822 Recruiting - Clinical trials for Peripheral Arterial Disease, Antiplatelet Therapy

Antiplatelet Strategy for Peripheral Arterial Interventions for Revascularization of Lower Extremities (ASPIRE PAD)

ASPIRE PAD
Start date: October 2014
Phase: Phase 3
Study type: Interventional

To evaluate whether clopidogrel 75 mg daily on a background of aspirin 75- 100 mg/d for 12 months or for 1 months will lead to an increased rate of primary patency, limb salvage, non-fatal myocardial infarction (MI), ischemic stroke, and survival, in patients receiving endovascular treatment of PAD at 1 year

NCT ID: NCT02307370 Completed - Clinical trials for Peripheral Arterial Disease

Atherectomy By Laser Ablation With Turbo-Elite

ABLATE
Start date: December 2014
Phase: N/A
Study type: Interventional

The primary objective for this study is to prove the safety and effectiveness of the Spectranetics Turbo-Elite catheter in atherectomy treatment for infrainguinal arteries with catheter to vessel sizing of at least 50%.

NCT ID: NCT02307292 Recruiting - Clinical trials for Peripheral Artery Disease

Prospective, Post Market Surveillance Q3-registry (POLARIS)

Q3-Registry
Start date: December 2014
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective, non-randomized post market surveillance registry designed to document the clinical Performance in Routine clinical practice of the POLARIS Peripheral Vascular Self Expanding Stent System

NCT ID: NCT02287831 Completed - Clinical trials for Peripheral Arterial Disease

Umbilical Cord Mesenchymal Stem Cells Injection for Peripheral Arterial Disease

Start date: February 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of umbilical cord blood mesenchymal stem cells with peripheral arterial disease.

NCT ID: NCT02280733 Recruiting - Clinical trials for Peripheral Arterial Disease

A Real World, Observational Registry of Chronic Wounds and Ulcers

USWR
Start date: January 2005
Phase:
Study type: Observational [Patient Registry]

More than 100 hospital based outpatient wound centers in the USA and Puerto Rico agree to transmit structured data on all patients followed with chronic wounds and ulcers (e.g. diabetic foot ulcers, venous ulcers, pressure ulcers, arterial ulcers, surgical wounds, and traumatic wounds). Data are collected at point of care including adherence to wound care quality measures developed by the USWR as a Qualified Clinical Data Registry (QCDR).

NCT ID: NCT02280200 Completed - Clinical trials for Peripheral Artery Disease

Ankle-foot Orthoses for Peripheral Artery Disease

Start date: November 2014
Phase: N/A
Study type: Interventional

The primary aim of this study is to investigate the effect of an ankle foot orthoses (AFO) on the primary outcome of peak walking time (PWT) in patients with peripheral artery disease (PAD).