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Arterial Occlusive Diseases clinical trials

View clinical trials related to Arterial Occlusive Diseases.

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NCT ID: NCT01075217 Completed - Clinical trials for Peripheral Arterial Occlusive Disease

Isovue in Peripheral Digital Subtraction Angiography (DSA)

Start date: April 2010
Phase: Phase 4
Study type: Interventional

No significant differences is expected in observed motion artifacts, heat or pain reported during peripheral DSA performed for diagnostic and/or endovascular therapeutic purposes.

NCT ID: NCT01007578 Completed - Atherosclerosis Clinical Trials

Drug-Eluting Balloon Catheters and the Treatment of Peripheral Arterial Occlusive Disease

Start date: September 15, 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine plasma levels of paclitaxel and catheter tolerability subsequent to treating patients with peripheral arterial occlusive disease (PAOD) with paclitaxel-coated balloon catheters.

NCT ID: NCT01002209 Withdrawn - Diabetes Clinical Trials

Postoperative Hyperbaric Oxygen Treatments to Reduce Complications in Diabetic Patients Undergoing Vascular Surgery

HODiVA
Start date: October 2019
Phase: Phase 2/Phase 3
Study type: Interventional

This trial aims to evaluate if hyperbaric oxygen treatment (HBO) given postoperatively is effective in reducing healing time and wound complications after lower extremity bypass surgery in patients with diabetes. Hypothesis: Postoperative HBO treatment is effective in reducing complications in patients with diabetes undergoing peripheral vascular surgery

NCT ID: NCT00940979 Terminated - Clinical trials for Arterial Obstructive Diseases

Trial Using Integuseal as Microbial Sealant for Arterial Bypass Surgery on Lower Extremities

ITT
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to prove a reduction of postoperative wound infections after direct preoperative use of a microbial sealant in the form of Integuseal for vascular procedures on lower extremities.

NCT ID: NCT00934037 Completed - Clinical trials for Coronary Artery Disease

Combined Non-invasive Coronary Angiography and Myocardial Perfusion Imaging Using 320 Detector Computed Tomography

Core320
Start date: December 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the diagnostic accuracy of multi-detector computed tomography using 320 detectors for identifying the combination of coronary artery stenosis ≥ 50% and a corresponding myocardium perfusion defect in a patient with suspected coronary artery disease compared with conventional coronary angiography and single photon emission computed tomography myocardium perfusion imaging.

NCT ID: NCT00927940 Completed - Clinical trials for Coronary Artery Disease

RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary Stent

RJ
Start date: March 2009
Phase: N/A
Study type: Interventional

The objective of the study is to verify the safety and efficacy of the MDT-4107 Drug-Eluting Coronary Stent for the treatment of de novo lesions in native coronary arteries.

NCT ID: NCT00913900 Terminated - Vascular Diseases Clinical Trials

Safety Study of Adult Stem Cells to Treat Patients With Severe Leg Artery Disease

SCRIPT-CLI
Start date: May 2009
Phase: Phase 1
Study type: Interventional

Peripheral artery disease (PAD) due to leg artery blockages can result in painful leg muscles, skin ulcers and infection due to poor blood flow. In severe forms, the only treatment may be amputation. Adult stem cells injected into affected legs may cause new blood vessel formation and improve blood flow. The purpose of this study is to determine the feasibility and safety of injecting adult stem cells into the leg muscles of patients with severe PAD, in an attempt to improve blood flow.

NCT ID: NCT00868972 Recruiting - Clinical trials for Renal Artery Obstruction

Renal Stenting With Distal Atheroembolic Protection

Start date: March 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Atherosclerotic renal artery stenosis (ARAS) is associated with progressive loss of renal function, refractory hypertension and flushing edema, responsible for mortality and morbidity, especially in the elderly. Current treatment includes restoration of the renal arterial lumen by endovascular stent placement and/or intensive medical therapy. There is no unanimous consent on which patients could benefice of the endovascular procedure due to the high rate of renal adverse events especially linked to atheroembolic disease. Recently, renal revascularization using a device which consents distal embolic protection of the kidney demonstrated to be a "safe" auxiliary procedure in a few non randomized studies. Interestingly atheromatous debris was detected in 60 to 80% of these devices analyzed after the procedure suggesting that these devices could prevent atheroembolism in a substantial proportion of patients. On the other hand, only a randomized controlled study can prove that renal stent with distal embolic protection is superior to renal stent alone in preserving kidney function. Therefore, the present study aims to compare the effects of renal artery stent placement with or without distal embolic protection on renal function in ARAS patients. Method: Patients with an ARAS of ≥70% and hypertension not responsive to at least 2 antihypertensive medications and/or renal failure (estimated GFR <60 mL/min/1.73 m2 are randomly assigned to stent placement alone or stent placement with distal embolic protection (FILTER WIRE EX; Cordis Endovascular, USA). Other medications consist of statins, anti-hypertensive drugs and antiplatelet therapy. Patients are followed for 3 months. The primary outcome of this study is a statistical significant difference in kidney function measured as Cr clearance and cystatin C level in the 2 groups at three months. The trial will include 150 patients.

NCT ID: NCT00863967 Active, not recruiting - Stroke Clinical Trials

Early Detection of Arteriosclerosis

Start date: October 2003
Phase: N/A
Study type: Observational

Arteriosclerosis is a common chronic disease with well known risk factors like diabetes mellitus, hypertension, dyslipidemia, adipositas and smoking, leading to severe complications like myocardial infarction, stroke or peripheral arterial occlusive disease. In addition to life-style factors there is also a genetic predisposition to develop complicated atherosclerosis. Objective: Improve individual risk prediction by clinical phenotyping and genotyping.

NCT ID: NCT00845585 Withdrawn - Clinical trials for Peripheral Arterial Occlusive Disease

Ovine Graft (Omniflow II) Versus PTFE in Below Knee Arterial Reconstruction

Start date: January 2009
Phase: N/A
Study type: Interventional

The study intends to compare commonly used PTFE grafts with the biologic ovine graft Ominiflow II for below-knee bypass surgery in patients with peripheral artery occlusive disease with no autologous vein graft available. The hypothesis of this randomized trial is that that Omniflow II does not have a higher patency than PTFE over 36 months (one-sided test). An interim analysis will be performed at 18