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Peripheral Vascular Disease clinical trials

View clinical trials related to Peripheral Vascular Disease.

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NCT ID: NCT00822172 Completed - Clinical trials for Peripheral Arterial Disease

Evaluation of Cilostazol in Combination With L-Carnitine

ECLECTIC
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see how safe and effective L carnitine taken with cilostazol is compared to placebo taken with cilostazol for people with intermittent claudication. A second purpose of the study is to see if L-carnitine is absorbed into the blood stream.

NCT ID: NCT00817349 Completed - Clinical trials for Coronary Artery Disease

Angio-Seal Evolution Device Registry

Start date: July 2008
Phase:
Study type: Observational

Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.

NCT ID: NCT00814970 Completed - Clinical trials for Peripheral Vascular Disease

The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions

Start date: November 2008
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Complete SE SFA Stent System in the treatment of de novo and/or restenotic lesions or occlusions in the Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) in subjects with symptomatic Peripheral Artery Disease (PAD).

NCT ID: NCT00764777 Completed - Clinical trials for Critical Limb Ischemia

Efficacy Study of Iliac Stents to Treat TASC A-B-C-D Iliac Artery Lesions

BRAVISSIMO
Start date: December 2008
Phase: Phase 4
Study type: Interventional

The BRAVISSIMO trial wants to investigate in a controlled setting, the long-term (up to 24 months) outcome of the self-expanding nitinol Absolute Pro (Abbott Vascular) and the balloon-expandable Omnilink Elite (Abbott Vascular) stent in TASC A&B and TASC C&D iliac lesions. A separate analysis of both patient populations will be performed and listed.

NCT ID: NCT00753337 Completed - Clinical trials for Peripheral Vascular Disease

The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study

ACTIVE
Start date: October 2008
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the safety and efficacy of the Assurant Cobalt Iliac Stent System in the treatment of de novo and restenotic lesions in iliac arteries of subjects with Peripheral Artery Disease (PAD).

NCT ID: NCT00751283 Withdrawn - Clinical trials for Peripheral Vascular Disease

Radiofrequency for the Treatment of Peripheral Vascular Occlusive Disease of the Lower Extremities

Start date: August 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the Minnow Medical GRST Peripheral Catheter System in the treatment of new lesions in the superficial femoral artery or the popliteal artery.

NCT ID: NCT00736086 Completed - Clinical trials for Cardiovascular Disease

RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System

Start date: March 2006
Phase: Phase 4
Study type: Observational

To evaluate early ambulation in patients who receive the StarClose™ VCS post-percutaneous diagnostic procedure.

NCT ID: NCT00730730 Completed - Clinical trials for Peripheral Vascular Disease

The Complete® Self-Expanding Stent and Stent Delivery System Registry

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to show if a new delivery system with a modified stent is safe in treating occluded iliac arteries in patients with peripheral vascular disease. The modified Complete SE delivery system is hypothesized to assist physicians with more accurate stent placement reducing the likelihood of stent 'jumping' seen with the use of many self-expanding stent systems.

NCT ID: NCT00721006 Completed - Clinical trials for Peripheral Artery Disease

Phase II Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia

MESENDO
Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to compare in patients with double-sided claudication if the transplant of a combination of stem cells obtained from the bone marrow of the same patient will contribute to the formation of new blood vessels in one of the severly diseased ischemic limbs(legs)versus the control limb that receives a placebo product. Limb Ischemia (LI) is a severe obstruction of the arteries which seriously decrease blood flow to the extremities (mainly feet and legs) and has progressed to the point of severe pain and even skin ulcers or sores. LI needs comprehensive treatment since the condition will not improve on its own. The overall goal of treatment is to reduce pain and increase blood flow to improve symptoms or save the leg and feet. In many cases, current options for treatment including medications, surgery or endovascular procedures have not been successful. In the last few years, investigators have explored therapies aimed to increase blood flow to the ischemic vessel by transplanting cells that will promote the development of new vessels in the diseased leg. The study hypothesis is based on the concept that the process of formation of new blood vessels is complex and requires the participation of several types of stem cells and growth factors. The lack of any of these components will produce vessels which are immature and unable to provide appropriated blood supply to the leg. Patients eligible to participate in the this study are those suffering from double-sided claudication with poor circulation or severe leg blockages, which are not candidates for surgical procedures. Once the mixture of stem cells is prepared and the patient's bone marrow is ready, cells will be transplanted into the calf muscle of one the the diseased legs while the other diseased leg will receive the placebo. Clinical study to evaluate and compare the efficacy of the stem cell transplant will be performed for six months post cell transplant.

NCT ID: NCT00667381 Completed - Clinical trials for Peripheral Vascular Disease

Femoral Arterial Access With Ultrasound Trial

FAUST
Start date: April 2008
Phase: N/A
Study type: Interventional

This study is designed to evaluate the routine use of vascular ultrasound as an aid for proper placement of a femoral arterial sheath during cardiac catheterization and peripheral arterial angiography.