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Vascular Diseases clinical trials

View clinical trials related to Vascular Diseases.

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NCT ID: NCT02464501 Completed - Clinical trials for Cardiovascular Disease

The OPC for Optimal Delivery of Paclitaxel for the Prevention of Endovascular Restenosis - Above and Below the Knee

COPPER-A
Start date: May 20, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of paclitaxel administration using the occlusion perfusion catheter (OPC) for the prevention of restenosis in infrainguinal de novo, restenotic femoropopliteal and infrapopliteal stenoses and occlusions, and in-stent restenosis.

NCT ID: NCT02458911 Completed - Clinical trials for Peripheral Vascular Disease

Luminor Registry: Registry of the Results of Angioplasty With Drug-eluting Balloon (Paclitaxel) in the Treatment of Infrainguinal Occlusive Lesions and Restenosis From Prior Endovascular Procedures in This Sector.

Start date: May 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of the study is to obtain data regarding safety and efficacy of drug-eluting balloon luminor 14 & luminor 35 in the treatment of infrainguinal occlusive lesions (superficial femoral artery (SFA), popliteal artery (PA) and tibial arteries (ATs)) and restenosis from prior endovascular procedures in this sector.

NCT ID: NCT02439775 Active, not recruiting - Hypertension Clinical Trials

SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-electrode Renal Denervation System

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to test the hypothesis that renal denervation decreases blood pressure and is safe when studied in the presence of up to three standard antihypertensive medications.

NCT ID: NCT02439749 Completed - Hypertension Clinical Trials

SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study

Start date: June 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to test the hypothesis that renal denervation decreases blood pressure and is safe when studied in the absence of antihypertensive medications.

NCT ID: NCT02436200 Completed - Clinical trials for Peripheral Vascular Disease

Neuromuscular Electrical Stimulation (NMES) in Patients With Intermittent Claudication

IC
Start date: December 2014
Phase: N/A
Study type: Interventional

This study will assess the benefit of a neuromuscular electrical stimulation device in patients suffering from symptoms and effects of lower limb intermittent claudication.

NCT ID: NCT02431234 Active, not recruiting - Clinical trials for Arteriosclerosis Obliterans

Arterial Calcification in the Diabetes

DIACART
Start date: February 2014
Phase:
Study type: Observational

The blood concentration of the protein RANKL could be predictive of the calcification of the leg arteries, which is a major complication occurring during diabetes. The objective of the DIACART study is to show that blood RANKL concentration predict the progression of calcification of the leg arteries in diabetic patients, independently of other cardiovascular risk factors.

NCT ID: NCT02429310 Completed - Clinical trials for Peripheral Vascular Disease

Adjuvant Benefit of NMES to Supervised Exercise in Patients With IC

AdjIC
Start date: December 2014
Phase: N/A
Study type: Interventional

This study will assess the adjuvant benefit of a neuromuscular electrical stimulation device to standard treatment of supervised exercise in patients suffering from symptoms and effects of lower limb Intermittent Claudication.

NCT ID: NCT02424383 Completed - Clinical trials for Peripheral Arterial Disease

Real-World Registry Assessing the Clinical Use of the Lutonix 035 Drug Coated Balloon Catheter

SAFE-DCB
Start date: April 23, 2015
Phase: N/A
Study type: Interventional

The objective of this patient registry is to assess the clinical use of the Lutonix 035 DCB PTA Catheter in a heterogeneous patient population in a real world and on-label clinical application.

NCT ID: NCT02418156 Completed - Clinical trials for Peripheral Vascular Disease

A Study on the Use of CorMatrix® ECM® for Femoral Arterial Reconstruction

PERFORM
Start date: May 2015
Phase:
Study type: Observational

To gather information on the use of CorMatrix ECM for Vascular Repair in the reconstruction of the femoral artery.

NCT ID: NCT02406131 Suspended - Clinical trials for Peripheral Vascular Diseases

Effects of Remote Ischemic Preconditioning on Restenosis Post Lower Limb Revascularization Angioplasty

Start date: April 2018
Phase: N/A
Study type: Interventional

The investigators will established relation between restenosis and inflammatory response to shearing stress caused by angioplasty suggest that any mechanism that affect inflammatory response can consequently affect the restenosis rate. There is accumulated evidence that remote ischemic precondition has modifying suppressive effect on inflammatory response and the investigators hypothesized that RIPC may lead to reduction in post angioplasty restenosis rate.