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Ischemia clinical trials

View clinical trials related to Ischemia.

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NCT ID: NCT02411266 Completed - Clinical trials for Ischemic Preconditioning

Preconditioning With Limb Ischemia for Subarachnoid Hemorrhage

PreLIMBS
Start date: July 30, 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to learn about protecting the brain from dangerous low blood flow.

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.

NCT ID: NCT02389946 Completed - Clinical trials for Coronary Artery Disease

Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions

BIOFLOW-V
Start date: May 2015
Phase: N/A
Study type: Interventional

The objective of this study is to assess the safety and efficacy of the Orsiro Sirolimus Eluting Coronary Stent System in the treatment of subjects with up to three native de novo or restenotic (standard PTCA only) coronary artery lesions compared to the Xience coronary stent system.

NCT ID: NCT02389647 Completed - Cerebral Ischemia Clinical Trials

Identification of Novel Molecular Markers for Cerebral Ischemia From Patients With Minor and Devastating Ischemic Injury

Start date: March 2015
Phase:
Study type: Observational

The purpose of this study is to use an iatrogenic model of stroke, meaning those strokes inadvertently caused by endovascular coiling of elective aneurysms, to study the biology of stroke in humans.

NCT ID: NCT02388867 Completed - Clinical trials for Critical Limb Ischemia

Matrix Metalloproteinases in Patients With Critical Limb Ischemia Undergoing Surgical Revascularization

ROMAMETA
Start date: January 2012
Phase: N/A
Study type: Interventional

In the present study the investigators will evaluate MMPs. serum levels variations in patients affected by critical limb ischemia, before and after lower limb surgical revascularization through venous or prosthetic bypass.

NCT ID: NCT02388061 Completed - Ischemic Stroke Clinical Trials

Tenecteplase Versus Alteplase Before Endovascular Therapy for Ischemic Stroke

EXTEND-IA TNK
Start date: March 23, 2015
Phase: Phase 2
Study type: Interventional

Patients presenting to the emergency department with acute ischemic stroke, who are are eligible for standard intravenous tPA therapy within 4.5 hours of stroke onset will be assessed for major vessel occlusion to determine their eligibility for randomization into the trial. If the patient gives informed consent they will be randomised 50:50 using central computerised allocation to intravenous alteplase or tenecteplase before all participants undergo intra-arterial clot retrieval. The trial is prospective, randomised, open-label, blinded endpoint (PROBE) design.

NCT ID: NCT02369809 Completed - Lower Limb Ischemia Clinical Trials

Non-Interventional Post Marketing Surveillance Study of Neovasculgen® in Patients With Chronic Lower Limb Ischemia

NVG-LIGHT
Start date: September 2012
Phase: Phase 4
Study type: Interventional

Aim of the study is to gain more knowledge about efficacy and safety of Neovasculgen® in daily clinical practice and obtain information about the quality of life in patients treated with Neovasculgen®.

NCT ID: NCT02360397 Completed - Myocardial Ischemia Clinical Trials

Ranolazine Mediated PVC Reduction in Ischemic Heart Disease

Start date: December 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether ranolazine has beneficial effects on cardiac ischemia through reduction of premature ventricular contraction burden.

NCT ID: NCT02351518 Completed - Cerebral Ischemia Clinical Trials

Cerebral Autoregulation and Vasospasm in Patients With TBI

Start date: November 2015
Phase:
Study type: Observational

Traumatic brain injury (TBI) affects 1.5 million patients per year in the United States, resulting in more than 50,000 deaths and more than 230,000 hospitalizations annually. Approximately 90,000 of these patients will suffer permanent impairment and more than half will experience short-term disability. Secondary injury processes play a critical role in the development of ischemia after trauma to the central nervous system and occur hours-to-days after the primary insult. Ischemia can lead to cerebral infarction or stroke. Ischemia has been described as the single most important secondary insult and has been identified histologically in approximately 90% of patients who die following closed head injury. Several factors resulting in post-traumatic cerebral ischemia have been identified: increased intracranial pressure (ICP), systemic arterial hypotension, and cerebral vasospasm. Cerebral vasospasm has been described as a sustained arterial narrowing. Clinically, the onset of new or worsening neurological symptoms is the most reliable indicator of cerebral vasospasm following a ruptured cerebral aneurysm. However, cerebral vasospasm is often unrecognized in patients suffering from moderate to severe TBI. These patients frequently have altered mental status due to the primary brain injury. In addition, they require narcotics for their pain and paralytics and/or sedatives while on a mechanical ventilator for airway protection. Thus, relying on the neurological exam to observe deteriorating neurological signs consistent with post-traumatic vasospasm (PTV) is reliable. While the etiology and outcome of patients with vasospasm secondary to ruptured aneurysm is well documented, the clinical significance of PTV after TBI is unknown. A better understanding of the role of cerebral autoregulation in the development of cerebral vasospasm could provide the answer. This proposal is for a pilot observational study describing the association of the impairment of cerebral autoregulation as measured by near infrared spectroscopy (NIRS) with the development of clinically significant vasospasm in patients with moderate to severe TBI. The information will serve as preliminary data for further study.

NCT ID: NCT02350283 Completed - Ischemic Stroke Clinical Trials

Endovascular Therapy for Acute Ischemic Stroke Trial

EAST
Start date: January 2015
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of Solitaire thrombectomy in Chinese patients with acute stroke within 12 hours of symptom onset.