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Peripheral Artery Disease clinical trials

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NCT ID: NCT02011984 Recruiting - Clinical trials for Peripheral Artery Disease

Multicentric Non-randomized Investigation of RESISTANT Camouflage Stent-system

RECAM
Start date: December 2013
Phase: N/A
Study type: Observational [Patient Registry]

Non-randomized multicenter post-market study to confirm the long-term safety and effectiveness of the CE-approved Camouflage-coated self-expandable RESISTANT Camouflage stent system for revascularization of de novo stenotic lesions in the superficial femoral artery in 100 compliant patients suitable for stent angioplasty. The CE-approved device will be used according to its intended use. Beyond the standard of care no further interventions are scheduled. Therefore, this trial is subject to the exception to the rule §23b of the German Medical Device Act (MPG), which includes the national implementation of EC directive 93/42/EEC.

NCT ID: NCT01969630 Recruiting - Clinical trials for Peripheral Artery Disease

Paclitaxel-eluting Balloon Angioplasty With Provisional Use of Nitinol Stent Versus Systematic Implantation of Paclitaxel-eluting Stent for the Treatment of Femoropopliteal de Novo Lesions

Start date: October 2013
Phase: Phase 4
Study type: Interventional

To determine in patients with symptomatic femoropopliteal lesions whether percutaneous revascularization with paclitaxel-eluting balloon angioplasty (PEB) and provisional nitinol stent is superior with respect to the 12-month incidence of restenosis compared to treatment with systematic paclitaxel-eluting stent (PES) angioplasty

NCT ID: NCT01960647 Recruiting - Clinical trials for Peripheral Artery Disease

FREERIDE STUDY, Freeway Paclitaxel Coated Balloon Catheter to Treat Peripheral Artery Disease

Start date: May 2011
Phase: Phase 3
Study type: Interventional

The primary objective of this prospective, Randomized, Controlled, Multicentre, Open Study is to investigate the inhibition of restenosis by the Paclitaxel-eluting Percutaneous transluminal angioplasty (PTA) balloon Freeway versus PTA alone in the treatment of de-novo occluded, stenotic or reoccluded, restenotic superficial femoral (SFA) or popliteal arteries.

NCT ID: NCT01499329 Recruiting - Clinical trials for Peripheral Artery Disease

Safety and Performance of the Zeus CC Stent for the Treatment of Iliac Occlusive Disease

EAZY
Start date: December 2011
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate safety and performance of the balloon-expandable Zeus CC (Rontis AG) stent for the treatment of Trans-Atlantic Inter-Society Consensus (TASC) A, B, C and D iliac lesions.

NCT ID: NCT01424020 Recruiting - Clinical trials for Peripheral Artery Disease

Walking Estimated Limitation Calculated by History - Study 2

WELCH-2
Start date: September 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test and validate a new questionnaire in order to get a "walking estimated limitation calculated by history (WELCH) in patients referred for vascular investigations.

NCT ID: NCT01095549 Recruiting - Clinical trials for Peripheral Artery Disease

Far Infrared Therapy on Peripheral Artery Disease in Hemodialysis Patients

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

The prevalence of peripheral artery disease (PAD) defined as ankle-brachial index (ABI) less than 0.9 was about 15~30% in patients with end stage renal disease (ESRD), which was higher than those with normal renal function. A lower ABI and a higher brachial-ankle pulse wave velocity (baPWV) are good markers to predict the risk of PAD and atherosclerosis respectively. In addition, baPWV>2,100 cm/s was shown to be related to potential PAD. ABI <0.9 was positively associated with vascular access failure in hemodialysis (HD) patients and our previous study has demonstrated that far infrared (FIR) therapy can improve access flow and unassisted patency of atrioventricular (AV) fistula. The aims of this study are to evaluate (1) the frequency of and (2) risk factors associated with abnormal ABI and PWV as well as (3) the effect of FIR on ABI and PWV and markers related to endothelial dysfunction in HD patients.

NCT ID: NCT00926081 Recruiting - Clinical trials for Peripheral Artery Disease

Exercise Training Versus Best Medical Treatment Only in Peripheral Artery Disease

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

The aim of the investigators' study is to analyze the value of supervised exercise training combined with medical therapy versus best medical treatment only with respect to quality of life. Furthermore, the investigators aim to evaluate the effect of supervised exercise training on microcirculation, peripheral endothelial progenitor cells as well as on future major cardiovascular adverse events.