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Arterial Occlusive Disease clinical trials

View clinical trials related to Arterial Occlusive Disease.

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NCT ID: NCT02255188 Completed - Clinical trials for ARTERIAL OCCLUSIVE DISEASE

Experimental Study of the Vascular Prosthesis Manufactured by Electrospinning

Start date: October 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether the Vascular prosthesis manufactured by Electrospinning is safe with respect to the development of thrombosis.

NCT ID: NCT02228564 Completed - Clinical trials for Peripheral Artery Disease

BARD® Study of LIFESTREAMâ„¢ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease

BOLSTER
Start date: September 2014
Phase: N/A
Study type: Interventional

Collect confirmatory evidence of the safety and effectiveness of the Balloon LIFESTREAMâ„¢ Stent Graft for the treatment of stenoses and occlusion in the iliac arteries.

NCT ID: NCT01746550 Completed - Clinical trials for Arterial Occlusive Disease

A Safety and Effectiveness Study of the MD-12-001 Stent in the Treatment of Superficial Femoral Artery or Popliteal Artery Blockages in Japanese Patients

Reliable
Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of the MD-12-001 stent in the treatment of superficial femoral artery and proximal popliteal artery blockages in Japanese patients.

NCT ID: NCT01548378 Completed - Clinical trials for Peripheral Vascular Disease

Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia

NL003CLI-II
Start date: March 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether intramuscular injections of NL003 into the calf is safe and effective in the treatment of critical limb ischemia

NCT ID: NCT01517997 Completed - Clinical trials for Arterial Occlusive Disease

Infrapopliteal Drug Eluting Angioplasty Versus Stenting

IDEAS-I
Start date: August 2011
Phase: Phase 2/Phase 3
Study type: Interventional

In total 50 patients diagnosed with long-segment infrapopliteal arterial disease will be randomized in two groups. The patients randomized in the Drug coated balloons (DCB) study arm will undergo a percutaneous transluminal angioplasty (PTA) with the use of a paclitaxel-coated balloon, while the patients randomized in the drug-eluting stent (DES) study arm will undergo primary stenting using drug-eluting stent(s). The study's primary endpoints will be the 6-month angiographic binary restenosis rate. Secondary endpoints will include the immediate technical success,6-month primary patency, target lesion revascularization and limb salvage and complication rates.

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: 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: 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: NCT00489320 Completed - Clinical trials for Cardiovascular Diseases

An Observational Registry Using Drug Eluting Stents (DES) in Patients in a Real-World Setting (DEScover Registry).

DESCOVER
Start date: December 2004
Phase: N/A
Study type: Observational

The DEScover Registry is designed to observe the results of using Drug Eluting Stents (DES) in patients in a real-world setting. The stents being observed are not investigational, that is, they have been approved for use in the general population.

NCT ID: NCT00447889 Completed - Clinical trials for Arterial Occlusive Disease

A Clinical Study of Gadoteric Acid in Non-Coronary Magnetic Resonance (MR) Angiography

Start date: March 2006
Phase: Phase 4
Study type: Interventional

This is a clinical study of gadoteric acid in non-coronary MR angiography.