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Arterial Occlusive Diseases clinical trials

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NCT ID: NCT02581150 Completed - Clinical trials for Peripheral Arterial Disease

Cost-utility Analysis of the Outpatient Versus Conventional Hospitalization in Treatment of Occlusive Arterial Disease

AMBUVASC
Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficiency of outpatient surgery compared to conventional hospitalization in endovascular treatment of occlusive arterial disease. A cost-utility analysis will be conducted from a societal perspective. Patients referred for peripheral arterial disease (PAD) will be randomized in two arms and a 3 months follow-up will be performed.

NCT ID: NCT02577796 Withdrawn - Arterial Occlusion Clinical Trials

Radial Artery Spasm Leading to Occlusion in Patients Undergoing Coronary Angiogram Via Radial Access

Start date: December 1, 2014
Phase:
Study type: Observational [Patient Registry]

Radial artery access is increasingly becoming popular among interventional cardiologists for patients undergoing percutaneous coronary intervention(PCI)/ diagnostic angiography secondary to its low complications rates. However, it is frequently associated with the spasm of the radial artery which can lead to difficulty in catheter manipulation during the procedure and potentially leading to vessel trauma. This vessel trauma can cause activation of coagulation system and formation of clot and subsequently the occlusion of radial artery. In this study the investigators intend to find the association of radial artery spasm with the future development of radial artery occlusion in patients who undergo PCI via radial access.

NCT ID: NCT02561000 Completed - Clinical trials for Coronary Artery Disease

Safety of PZ-128 in Subjects Undergoing Non-Emergent Percutaneous Coronary Intervention

TRIP-PCI
Start date: May 27, 2016
Phase: Phase 2
Study type: Interventional

The object of the study is to determine whether different doses of PZ-128, when added to standard medical care in persons undergoing cardiac catheterization/percutaneous coronary intervention, will increase the risk of bleeding. A secondary objective is to determine whether patients treated with PZ-128 have fewer cardiac events such as heart attack, bypass surgery or stroke compared with those persons treated with the standard of care.

NCT ID: NCT02531230 Completed - Clinical trials for Peripheral Arterial Occlusive Disease

"All Comers" Post Market Clinical Follow-up (PMCF) With Multi-LOC for flOw liMiting Outcomes

LOCOMOTIVE
Start date: July 2015
Phase:
Study type: Observational

The aim of the study is to assess the safety and efficacy of the Multi-LOC® peripheral stent system to treat de novo and restenotic lesions (no in-stent restenosis (ISR), no restenosis post drug coated balloon (DCB) after flow limiting plain old balloon angioplasty (POBA) and/or DCB dilatations in the superficial femoral artery (SFA) and popliteal segments (P1, P2 & P3)

NCT ID: NCT02465125 Completed - Anemia Clinical Trials

The Transfusion Triggers in Vascular Surgery Trial

TV
Start date: July 15, 2015
Phase: Phase 2
Study type: Interventional

BACKGROUND - Vascular surgical patients often receive red blood cell (RBC) transfusions in the peri-operative period - RBC transfusion may lead to improved outcome but on the other hand the intervention may be harmful - Danish Health and Medicines Authority recommends transfusion of RBC at hemoglobin below 5 mmol/L while local clinical guidelines recommend transfusion of RBC to maintain hemoglobin levels above 6 mmol/L - A large randomized clinical trial is needed to evaluate the efficacy and safety of RBC transfusion in patients undergoing vascular surgery. - A trial examining the effect of RBC transfusion on tissue oxygenation is used to test the trial-design and feasibility for a trial evaluating post-operative mortality and morbidity.

NCT ID: NCT02460042 Active, not recruiting - Clinical trials for Peripheral Arterial Occlusive Disease

Clinical Post Market Clinical Follow-up (PMCF) on Peripheral Arteries Treated With SeQuent® Please Over The Wire (OTW)

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

The aim of the study is to assess the safety and efficacy of the paclitaxel-releasing balloon catheter SeQuent® Please OTW to treat de novo and restenotic lesions in peripheral arteries. It is the intention of this trial to treat suitable target lesions with drug coated balloon (DCB) only.

NCT ID: NCT02455726 Not yet recruiting - Clinical trials for Peripheral Arterial Disease

Magnesium Oral Supplementation to Reduce Pain Inpatients With Severe Peripheral Arterial Occlusive Disease

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

Magnesium exerts analgesic effects in several animal pain models and in patients affected by acute postoperative pain and chronic pain of neuropathic origin. There is no evidence that magnesium can modulate pain in patients with peripheral arterial occlusive disease (PAOD). We describe the protocol of a single-center randomized double-blind clinical trial aimed at assessing the efficacy of oral magnesium supplementation in controlling severe pain in patients with advanced PAOD.

NCT ID: NCT02441556 Completed - Clinical trials for Stroke Due to Basilar Artery Occlusion

Acute Basilar Artery Occlusion: Endovascular Interventions vs Standard Medical Treatment

BEST
Start date: January 2015
Phase: N/A
Study type: Interventional

This trial will provide valuable insights into the safety and efficacy of endovascular treatment for acute ischemic stroke patients with basilar artery occlusion within 8 hours of estimated occlusion time.

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: NCT02395744 Completed - Clinical trials for Cardiovascular Diseases

The COPPER-B Trial

COPPER-B
Start date: March 11, 2015
Phase: N/A
Study type: Interventional

The purpose of the COPPER - B study is to assess the feasibility, safety, and initial efficacy of paclitaxel administration using the OPC for the prevention of restenosis in infrapopliteal de novo and restenotic lesions and occlusions using a novel catheter, the OPC.