Clinical Trials Logo

Peripheral Vascular Diseases clinical trials

View clinical trials related to Peripheral Vascular Diseases.

Filter by:

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: 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: 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: NCT02276781 Completed - Clinical trials for Peripheral Arterial Disease

BRAVO: Biomarker Risk Assessment in Vulnerable Outpatients

BRAVO
Start date: September 2009
Phase: N/A
Study type: Observational

The investigators hypothesize that among people with lower extremity peripheral artery disease (PAD), biomarker levels are higher during time periods immediately preceding an acute coronary event compared to time periods not immediately preceding an acute coronary event. Biomarkers the investigators will study are CRP, SAA, and D-dimer. Biomarkers will be measured at baseline and every two months during follow-up. The primary aims of this study are as follows. Specific Aim #1. Among participants with PAD who experience an acute coronary event during follow-up, the investigators will determine whether biomarker levels measured immediately prior to the coronary event are higher than levels that do not immediately precede coronary events. Specific Aim #2, Part 1. The investigators will determine whether participants who experience a coronary event (cases) have higher biomarker levels at the visit immediately prior to the event than participants who have not experienced a coronary event (controls) at the time of the case event. Specific Aim #2, Part 2. The investigators will determine whether participants who experience a coronary event (cases) have a greater increase in biomarkers during the time period leading up to the event compared to participants who have not experienced a coronary event (controls). To achieve these aims, the investigators will enroll up to 650 participants with PAD and follow them prospectively, measuring blood samples every two months, and ascertaining the presence of acute coronary events every two months.

NCT ID: NCT02273232 Completed - Clinical trials for Peripheral Arterial Diseases

Effects of Remote Ischemic Preconditioning on Moderate PVD Patients A Pilot Randomized Control Trial

RIPC-PVD
Start date: January 2015
Phase: Phase 1
Study type: Interventional

Remote ischemic Preconditioning (RIPC) is a phenomena first observed in cardio-thoracic patients in which exposing the limbs for periods of short intermittent ischemia produces protective effect on heart muscle. The concept was applied to many other parts of the body and the results are positive so far. No human trials on this concept has been conducted in patients with peripheral vascular disease so far but applying the concept for healthy individuals shows vessels dilatation and animal trials shows degree of new vessels formation in addition to reports of symptoms improvement. The trial candidates will be allocated blindly in 4 groups. All groups will have advice about exercise which is the standard practice now. The first group will have supervised exercise. The second group will in addition to the supervised exercise get the ischemic preconditioning with the blood pressure cuff. The third group will get the ischemic preconditioning and the fourth group will get the standard exercise advice. All candidates will have Magnetic Resonance Image Scan (MRA) for their blood vessels in the beginning of the trial and again at the end. The effect of the RIPC (Remote ischemic Preconditioning) and exercises on patient symptoms, new vessel formation and other parameters will be recorded

NCT ID: NCT02271529 Completed - Clinical trials for Peripheral Vascular Disease

Zilver PTX Delivery System

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

The objective of this study is to evaluate the performance of the Zilver PTX stent thumbwheel delivery system.

NCT ID: NCT02254837 Completed - Clinical trials for Peripheral Arterial Disease (PAD)

Zilver PTX Post-Market Study in Japan

Start date: May 2012
Phase: N/A
Study type: Interventional

Japanese post market clinical study of the Zilver PTX device.

NCT ID: NCT02254356 Completed - Clinical trials for Peripheral Arterial Disease (PAD)

Zilver Flex Post-Market Study in Japan

Start date: May 2012
Phase: N/A
Study type: Interventional

Japanese post market clinical study of the Zilver Flex device.

NCT ID: NCT02246660 Completed - Clinical trials for Peripheral Arterial Disease

RESveratrol To Improve Outcomes in oldeR pEople With PAD (the RESTORE Trial)

RESTORE
Start date: January 2015
Phase: N/A
Study type: Interventional

The RESTORE trial will determine whether resveratrol supplementation can improve walking performance in older people with lower extremity peripheral arterial disease (PAD). Resveratrol, a polyphenol and natural supplement, specifically targets several impairments associated with walking difficulty and mobility loss in people with PAD.

NCT ID: NCT02228564 Completed - Clinical trials for Peripheral Artery Disease

BARD® Study of LIFESTREAMâ„¢ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease

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

Collect confirmatory evidence of the safety and effectiveness of the Balloon LIFESTREAMâ„¢ Stent Graft for the treatment of stenoses and occlusion in the iliac arteries.