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Ischemia clinical trials

View clinical trials related to Ischemia.

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NCT ID: NCT03892226 Active, not recruiting - Stroke, Ischemic Clinical Trials

Cardiomyocyte Injury Following Acute Ischemic Stroke

CORONA-IS
Start date: April 1, 2019
Phase:
Study type: Observational

The primary goal of the CORONA-IS study is to characterize stroke-associated acute myocardial injury (elevated hs-cardiac troponin) using different diagnostic examinations in order get a better understanding of it's underlying pathomechanisms.

NCT ID: NCT03810469 Active, not recruiting - Clinical trials for Peripheral Arterial Disease

Foot Perfusion Analysis to Predict Limb Salvage

DELTA-PERF
Start date: February 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study aims at evaluating the correlation between foot perfusion on angiographies performed before and after revascularization and limb salvage in patients with critical limb ischemia.

NCT ID: NCT03807661 Active, not recruiting - Clinical trials for Critical Limb Ischemia

Percutaneous Deep Vein Arterialization Post-Market Study

PROMISE UK
Start date: December 11, 2019
Phase: N/A
Study type: Interventional

The objective of this post-market study is to evaluate the safety and effectiveness of the LimFlow System in creating a below-the-knee arterio-venous fistula for venous arterialization in subjects with critical limb ischemia.

NCT ID: NCT03685006 Active, not recruiting - Inflammation Clinical Trials

Atherosclerosis and Acute Ischemic Stroke Study

Start date: January 1, 2009
Phase:
Study type: Observational [Patient Registry]

A significant proportion of strokes are thromboembolic in nature, arising from atherosclerotic plaque at the carotid bifurcation. It is now wellknown that inflammation plays a key role in atherogenesis and plaque destabilization. However the identification and characterization of the different inflammatory factors, as well as their relative importance, have not been clarified. This main aim of this study is to identify new risk markers for atherosclerosis and to characterize more precise methods for detection of the unstable carotid plaque with increased stroke-risk.

NCT ID: NCT03684564 Active, not recruiting - Stroke Clinical Trials

RIvaroxaban for Stroke Patients With AntiPhospholipid Syndrome

RISAPS
Start date: July 9, 2021
Phase: Phase 2
Study type: Interventional

Rivaroxaban versus warfarin for stroke patients with antiphospholipid syndrome, with or without SLE (RISAPS): a randomised, controlled, open-label, phase IIb, non-inferiority proof of principle trial. 40 patients will be randomised with a ratio of 1:1 to receive either: - Rivaroxaban 15mg twice daily orally for 24 months or - Warfarin (standard of care in the RISAPS trial) to maintain a target INR of 3.5 (range 3.0-4.0) for 24 months. The primary outcome of the trial is the rate of change in brain white matter hyperintensity (WMH) volume between baseline and 24 months follow up, assessed on brain magnetic resonance imaging (MRI), a surrogate marker of ischaemic damage.

NCT ID: NCT03679572 Active, not recruiting - Renal Cancer Clinical Trials

Zero-ischemia Robot-assisted Partial Nephrectomy Using Near-infrared Fluorescence

EMERALD
Start date: February 5, 2018
Phase: N/A
Study type: Interventional

Patients with renal cancer are commonly treated by robot-assisted partial nephrectomy. Renal artery clamping is commonly required inducing kidney ischemia during surgery. It impacts parenchymal and renal function. This study aims to compare a new surgical procedure in order to reduce ischemia effect and preserve renal function after partial nephrectomy for renal tumour.

NCT ID: NCT03663543 Active, not recruiting - Clinical trials for Ischemia Reperfusion Injury

Intravenous Estrogen in Kidney Transplant Study

PERT
Start date: August 26, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Ischemia perfusion injury (IRI) is a major cause of organ injury during kidney transplantation. Currently there are no treatments for IRI other than dialysis. Preliminary studies in female mice have found protection from IRI when given short term estrogen supplements. This study will look at the effect of intravenous estrogen given peri-operatively to reduce the effect of IRI in female kidney transplant recipients.

NCT ID: NCT03656848 Active, not recruiting - Clinical trials for Coronary Artery Disease

The FAVOR III China Study

FAVORIII
Start date: December 25, 2018
Phase: N/A
Study type: Interventional

The overall purpose of the FAVOR III China trial is to investigate if a strategy of quantitative flow ratio (QFR)-guided percutaneous coronary intervention (PCI) yields superior clinical outcome and cost-effectiveness compared to a strategy of standard coronary angiography-guided PCI in evaluation of patients with coronary artery disease.

NCT ID: NCT03653312 Active, not recruiting - Ischemic Stroke Clinical Trials

Neuromuscular Electrical Stimulation in Acute Ischemic Stroke

NESA
Start date: August 27, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to examine the added effect of NeuroMuscular Electric Stimulation (NMES) in addition to exercise therapy in the acute phase of ischemic stroke. This randomized controlled trial includes 50 patients allocated to either control or intervention. The inclusion, test, training and re-test will be provided during the first 14 days after ictus, starting day 1 or 2 after ictus and a follow-up at day 90. The exercise training with external NMES is done with the patient every weekday for 12 minutes.

NCT ID: NCT03519737 Active, not recruiting - Clinical trials for Acute Ischemic Stroke

Aureva Transcranial Ultrasound Device With tPA in Patients With Acute Ischemic Stroke

TRUST
Start date: August 17, 2018
Phase: N/A
Study type: Interventional

This is a randomized, placebo controlled, double-blind phase 3 clinical study to evaluate the efficacy and safety of transcranial ultrasound (TUS) using the Sonolysis Headframe as an adjunctive therapy to intravenous (IV) tissue plasminogen activator (tPA) therapy in subjects with acute ischemic stroke that initially present at non-endovascular (EVT) treating hospitals that have established transport services in place to transfer subjects to hospitals capable of performing EVT.