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Arterial Occlusive Diseases clinical trials

View clinical trials related to Arterial Occlusive Diseases.

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NCT ID: NCT00740207 Completed - Clinical trials for Peripheral Arterial Occlusive Disease

Pilot Study to Compare ISOVUE®-250 and VISIPAQUEâ„¢ 270 for Motion Artifact and Pain in Peripheral DSA

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

The purpose of this study is to compare ISOVUE-250 and VISIPAQUE 270 for motion artifact and pain following intraarterial injection for peripheral DSA.

NCT ID: NCT00673985 Completed - Clinical trials for Intermittent Claudication

Edwards Lifesciences Self-Expanding Stent Peripheral Vascular Disease Study

RESILIENT
Start date: July 2004
Phase: N/A
Study type: Interventional

The main objective of this study is to assess the safety and effectiveness of the Edwards Lifesciences LifeStent nitinol self expandable stent device and its delivery system in the treatment of occlusive superficial femoral artery (SFA) disease by reducing the re-intervention rate as compared to percutaneous transluminal angioplasty (PTA) alone

NCT ID: NCT00664963 Completed - Clinical trials for Arterial Occlusive Diseases

YUKON-drug-eluting Stent Below The Knee - Randomised Double-blind Study

YUKON-BTK
Start date: April 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness of the treatment with balloon-expandable YUKON-BTX-Sirolimus-eluting stent over the treatment with YUKON-BTX uncoated stent in patients with ischemic infrapopliteal arterial disease.

NCT ID: NCT00660634 Completed - Clinical trials for Intermittent Claudication

Angioplasty in Peripheral Arterial Disease and Endothelial Function

PTA-PAD-FMD
Start date: December 2004
Phase: Phase 4
Study type: Interventional

To investigate whether endovascular revascualrization of infrainguinal arterial obstructive disease has an effect on brachial artery reactivity

NCT ID: NCT00619788 Completed - Clinical trials for Peripheral Arterial Occlusive Disease

FeMoropopliteal AngioSculptâ„¢ SCoring BallOon CaTheter Study

MASCOT
Start date: March 2008
Phase: Phase 2/Phase 3
Study type: Interventional

This investigation is designed to demonstrate the efficacy and safety of the 4.0-5.0mm AngioSculpt Scoring Balloon Catheter (AngioScore, Inc.) for femoropopliteal use in a controlled clinical investigation. The scoring balloon is a semi-compliant balloon encircled by 3 spiral struts with a nitinol scoring element, which theoretically provides targeted scoring of lesions, by concentrating the dilation force thus minimizing barotrauma, elastic recoil and uncontrolled dissection. This may improve the outcome of the intervention and reduce the number of stents required.

NCT ID: NCT00614848 Completed - Clinical trials for Coronary Artery Disease

The ENDEAVOR II Clinical Trial: The Medtronic Endeavor Drug Eluting Coronary Stent System in Coronary Artery Lesions

ENDEAVOR II
Start date: June 2003
Phase: N/A
Study type: Interventional

To demonstrate the safety and efficacy of the Driver Coronary Stent coated with 10 mcg/mm ABT-578 compared to the uncoated Driver Stent for the treatment of single de novo lesions in native coronary arteries 2.25-3.5 mm in diameter.

NCT ID: NCT00596752 Completed - Clinical trials for Peripheral Arterial Occlusive Disease

Alprostadil in Peripheral Arterial Occlusive Disease (PAOD) Stage IV

ESPECIAL
Start date: March 2004
Phase: Phase 4
Study type: Interventional

The study is to confirmatorily show a superior effect of Alprostadil compared to placebo on the rate of complete healing of ischemic necroses and ulcerations as well as on the frequency and height of major amputations in patients suffering from PAOD stage IV.

NCT ID: NCT00595257 Completed - Clinical trials for Arterial Occlusive Diseases

Feasability Study of Autologous Bone Marrow Aspirate Concentrate for Treatment of CLI

Start date: December 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if concentrated nucleated cells from your own bone marrow, injected or infused into an ischemic limb, will restore sufficient blood flow to avoid amputation.

NCT ID: NCT00537498 Completed - Diabetic Foot Clinical Trials

Urokinase Therapy in Diabetic Foot Syndrome

Start date: February 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether a treatment with urokinase (500 000 or 1 000 000 IU) can lead to ulcer-healing, lower rate of major amputation, and prolonged survival in patients with diabetic foot syndrome.

NCT ID: NCT00523263 Completed - Clinical trials for Intermittent Claudication

Dacron vs Dardik for Fem-Pop Bypass

DaDa
Start date: January 1996
Phase: Phase 3
Study type: Interventional

Clinical trial for the comparison of long-term patency of heparin-bonded Dacron and human umbilical vein vascular prostheses in above-knee femoro-popliteal bypass surgery.