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Peripheral Arterial Disease clinical trials

View clinical trials related to Peripheral Arterial Disease.

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NCT ID: NCT00378040 Completed - Clinical trials for Peripheral Vascular Disease

Systematic Assessment of Vascular Risk

Start date: June 2004
Phase: N/A
Study type: Observational

It is hypothesized that patients with vascular disease are undertreated for modifiable risk factors, leading to increased morbidity and mortality in this population. The objective of this study is to develop a comprehensive database that will demonstrate the current adequacy of risk factor management in this high risk population, and that will provide needed guidance for future treatment options.

NCT ID: NCT00371371 Completed - Ischemia Clinical Trials

Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI)

JUVENTAS
Start date: September 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purposes of this study are to determine whether intra-arterial injection of autologous stem cells is effective in the treatment of chronic limb ischemia (CLI), to characterize stem cell dysfunction in patients with CLI, and to relate the stem cell function with clinical outcome.

NCT ID: NCT00368797 Completed - Clinical trials for Peripheral Arterial Disease

Efficacy and Safety Study of NV1FGF in Patients With Severe Peripheral Artery Occlusive Disease

TALISMAN 201
Start date: March 2002
Phase: Phase 2
Study type: Interventional

This study is a double-blind study to evaluate the efficacy and safety of NV1FGF, a pCOR plasmid constructed by inserting the gene coding for the FGF compared to placebo in patients with severe Peripheral Arterial Occlusive Disease, Fontaine's stage IV. The efficacy was assessed by the complete healing of at least one ulcer in the treated limb, 25 week post-baseline and secondary by the rate of amputation and death.

NCT ID: NCT00355537 Completed - Diabetes Mellitus Clinical Trials

Testosterone Replacement in Diabetes With Vascular Disease (Version 2)

Start date: February 2006
Phase: Phase 4
Study type: Interventional

Diabetes is a major cause of peripheral vascular disease(PVD) and is associated with male hypogonadism. Diabetes and PVD are both associated with arterial stiffness and intima -media thickness which are also related to severity of the clinical syndrome of PVD. Artificially induced hypogonadism results in increasing arterial stiffness whilst testosterone is known to improve risk factors for vascular disease and act as a vasodilator. The purpose of this pilot study is to assess the effect of testosterone treatment on PVD arterial stiffness and intima-media thickness in men with type 2 diabetes and hypogonadism,

NCT ID: NCT00300339 Completed - Clinical trials for Intermittent Claudication

Mixed Antagonist of Serotonin for Claudication Optimal Therapy

MASCOT
Start date: February 2006
Phase: Phase 2
Study type: Interventional

To investigate in patients suffering from intermittent claudication due to Fontaine stage II PAD whether a 24-week treatment by SL650472 OD on top of clopidogrel may result in an improvement of walking capacity, by comparing three doses of SL650472 to placebo, and to calibrate such effect versus cilostazol

NCT ID: NCT00296855 Completed - Clinical trials for Peripheral Vascular Diseases

Comparison Study of Vasovist® Magnetic Resonance Angiography (MRA) and an MRA With a Conventional Extracellular Contrast Agent With X-ray Angiography in Patients With Peripheral Artery Disease

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The particular aim of this study is the comparison of the diagnostic results of MRA images upon application of Vasovist (gadofosveset), a contrast agent not yet available on the market, with the MRA images upon application of a conventional extracellular contrast agent. A catheter angiography, which will be performed as a routine diagnostic procedure for vascular diseases, will serve as an evaluation standard.

NCT ID: NCT00284076 Completed - Clinical trials for Cardiovascular Diseases

L-Arginine in the Treatment of Peripheral Arterial Disease

Start date: February 2000
Phase: N/A
Study type: Interventional

To assess the effects of L-arginine upon functional status (treadmill exercise testing; quality of life) and limb blood (by mercury strain gauge plethysmography) in peripheral arterial disease.

NCT ID: NCT00282646 Completed - Clinical trials for Arterial Occlusive Diseases

Safety and Feasibility Study of Autologous Bone Marrow Cell Transplantation in Patients With Peripheral Arterial Occlusive Disease (PAOD)

Start date: October 2005
Phase: Phase 2
Study type: Interventional

Patients with peripheral artery disease, stage III or IV who are not candidates for interventional or operative therapy should be treated with intraarterial progenitor cell therapy (autologous bone marrow cells) in a randomized, placebo controlled trial.

NCT ID: NCT00278603 Completed - Clinical trials for Peripheral Vascular Disease

Stem Cell Injection for Peripheral Vascular Disease

Start date: October 2004
Phase: Phase 1
Study type: Interventional

Severe peripheral vascular disease of the legs causes narrowing of the blood vessels in the legs, which keeps the blood from flowing adequately through these vessels. This study is designed to examine whether treating patients with their own previously collected blood stem cells will improve blood flow in the most severely affected leg. Blood stem cells are undeveloped cells that have the capacity to grow into mature blood cells, which normally circulate in the blood stream.

NCT ID: NCT00232869 Completed - Clinical trials for Peripheral Artery Disease

A Study of the SMART Stent in the Treatment SFA Disease.

SIROCCO
Start date: February 2001
Phase: Phase 2
Study type: Interventional

The main objective of this study is to assess the safety and performance of the sirolimus coated Cordis SMARTâ„¢ nitinol self expandable stent device and its delivery system in the treatment of obstructive superficial femoral artery (SFA) disease in reducing percent in-stent mean lumen diameter stenosis in de novo or restenotic native lesions as compared to the uncoated SMARTâ„¢ stent.