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Vascular Diseases clinical trials

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NCT ID: NCT00837330 Completed - Clinical trials for Polypoidal Choroidal Vasculopathy

Ranibizumab (Lucentis) for Polypoidal Choroidal Vasculopathy

Start date: May 2006
Phase: Phase 1/Phase 2
Study type: Interventional

This Phase I/II safety study is designed to investigate the safety and efficacy of ranibizumab (Lucentis) in the treatment of polypoidal choroidal vasculopathy (PCV), a potentially blinding eye disease that involves the growth of tiny, abnormal blood vessels under the retina. These abnormal blood vessels can bleed or leak fluid, causing disruption of normal retinal function and vision loss. Ranibizumab is a drug that is FDA-approved for the treatment of wet age-related macular degeneration (AMD) and is injected directly into the eye. Given the efficacy of ranibizumab in the treatment of wet AMD, and the postulated similarity between the disease mechanisms involved in both wet AMD and PCV, we believe ranibizumab will have a beneficial effect on visual function in patients with PCV.

NCT ID: NCT00830570 Completed - Clinical trials for Venous Thromboembolism

The Clinical and Economic Impact of Pharmacogenomic Testing of Warfarin Therapy in Typical Community Practice Settings

MHSMayoWarf1
Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this quasi-experiment study, which could also be classified as a prospective observational intervention study, is to assess the impact of cytochrome P450 2C9 (CYP 2C9) and vitamin K epoxide reductase complex, subunit 1 (VKORC1) testing within a primary patient care setting.

NCT ID: NCT00829361 Completed - Stroke Clinical Trials

Stroke Telemedicine for Arizona Rural Residents Trial

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

The STARR network registry consists of a 4 spoke 1 hub system. Which will consist of prospective collection, recording, and regular analysis of telestroke patient consultation and care data for the purpose of quality measure assessment and improvement and benchmarking against other national and international telestroke programs.

NCT ID: NCT00827853 Completed - Clinical trials for PERIPHERAL VASCULAR DISEASE

Study Comparing Two Methods of Expanding Stents Placed in Legs of Diabetics With Peripheral Vascular Disease

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

Despite recent advances in stent technology and its widespread application in the treatment of peripheral vascular disease (PVD), incidences of partial or complete blockage of stent lumen (in-stent restenosis) due to in growth of cells (neo-intimal proliferation) is unacceptably high. In diabetics with long superficial femoral artery (SFA) lesions, in-stent restenosis rates are higher than in non-diabetics. Consequently interventional techniques that curtail in-stent restenosis have to be explored. Cryoplasty is a stent expansion method in which a balloon is expanded using pressurized nitrous oxide gas. As the nitrous oxide expands in the balloon it cools the surroundings to about -10 degrees C. This induces programed death (apoptosis) of the smooth muscle cells in arterial wall. The investigators hypothesize that Cryoplasty, by inducing an apoptotic smooth muscle cell response, when applied to post-dilation of nitinol self-expanding stents in the Superficial Femoral Artery (SFA) of diabetics, would lead to decreased in-stent restenosis due to decreased neointimal proliferation.

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: NCT00805831 Completed - Atherosclerosis Clinical Trials

Safety and Efficacy of Using HDH Device and Method - a Novel Sutureless Vascular Anastomosis

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

The HDH device is intended for creating sutureless vascular anastomosis in various blood vessels. The HDH device consists of four parts: an elastic tube (graft), docking head (anastomotic device), inversion device (connects the vascular graft to HDH) and measuring device. This study was design in order to evaluate the safety and efficacy of using HDH device and method an innovative anastomotic device for sutureless aortic anastomosis in patient diagnosed with abdominal aneurysm or Aorto-iliac aneurysm.

NCT ID: NCT00804024 Completed - Heart Diseases Clinical Trials

ClearWay™ RX Registry Trial

Start date: August 2008
Phase: N/A
Study type: Observational [Patient Registry]

The primary goal of this registry is to collect data regarding the use of the ClearWay RX Local Therapeutic Infusion Catheter for all indications.

NCT ID: NCT00797056 Completed - Clinical trials for Peripheral Vascular Diseases

Stem Cell Mobilization by G-CSF to Treat Severe Peripheral Artery Disease

STEMPAD
Start date: April 2008
Phase: Phase 0
Study type: Interventional

This study is designed to test the use of G-CSF in peripheral vascular disease. The investigators hypothesize that mobilization of angiogenic cells into the blood by granulocyte colony stimulating factor (G-CSF) may stimulate the formation of new blood vessels and result in a sustained improvement in blood flow in patients with severe peripheral arterial disease.