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Ischemia clinical trials

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NCT ID: NCT02834858 Recruiting - Diabetic Foot Clinical Trials

Umbilical Cord Mesenchymal Stem Cells Infusion for Diabetes Related Vascular Complications

Start date: January 2016
Phase: Phase 1
Study type: Interventional

Stem cell therapy has been a new and effective therapy in recent years for diabetic foot.This study intends to establish an optimal clinical research program, and attempts to break the technical bottleneck in the stem cell therapy for treating diabetes related vascular complications.

NCT ID: NCT02834351 Completed - Clinical trials for Peripheral Artery Disease

Tissue Lesions in Exercise Related Ischemia

SARTORIUS
Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of muscle ischemia during claudication on mitochondrial function. Comparison to patients with arterial disease but absence of lower limb claudication (Cardiac group) feasibility study.

NCT ID: NCT02834143 Completed - Stroke Clinical Trials

Evaluation of Diagnostic Criteria for Chronic Critical Limb Ischemia

CRIMI
Start date: June 13, 2014
Phase: N/A
Study type: Observational

Chronic critical limb ischemia (CCI) is the most severe clinical form of occlusive arterial disease. Its prognosis is terrible, mortality estimated at 50% in five years. However there are no recent epidemiological data on morbidity and mortality of critical ischemia. Moreover, the diagnostic criteria of the ICC associate clinical and hemodynamic criteria and are not subject to a clear consensus. Investigators propose to evaluate the validated diagnostic criteria (TASC VALMI, European working group) in a population of severe ischemia in patients in order to offer relevant simple and reproducible criteria. Secondly Investigators propose to monitor the medium and long term evolution of these patients ICC defined to clarify the prognosis. diagnostic criteria of the different societies: - TASC: Transatlantic criteria: very characteristic pain, wound optional, variable hemodynamic criteria as the presence of a wound or not - VALMI: French criteria derived vascular medical college: characteristic pain, sore, hemodynamic reproducible, reliable criteria - European working group: European definition of criteria, including a characteristic pain, requires no wound, different hemodynamic criteria of 2 others.

NCT ID: NCT02833688 Completed - Clinical trials for Ischemia-reperfusion Injury

Effects of Dexmedetomidine on the Liver Injury After Hepatectomy

Start date: August 2, 2016
Phase: Phase 4
Study type: Interventional

To investigate whether dexmedetomidine reduce liver injury after hepatectomy. During hepatectomy, surgeons always took inflow occlusion to reduce blood loss with Pringle maneuver. A few clinical studies had shown dexmedetomidine could reduce ischaemia/reperfusion (IR) injury caused by the secretion of reactive oxygen species and inflammatory cytokines. Glutathione-S-transferase (GST) was a sensitive and specific marker for hepatic injury in several studies before. So the investigator decided to use it as the primary endpoint. Besides, in our center, there are some liver resection surgeries that didn't need occlusion. So it can serve the best placebo for determine the the actual effect of dexmedetomidine on the IR injury in further subgroup analysis.

NCT ID: NCT02831088 Recruiting - Ischemic Stroke Clinical Trials

Safety and Optimal Neuroprotection of neu2000 in Ischemic Stroke With Endovascular reCanalizion (SONIC)

SONIC
Start date: July 2016
Phase: Phase 2
Study type: Interventional

Efficacy and safety of Neu2000, a multi-target drug designed to prevent both NMDA receptor-mediated excitotoxicity and free radical toxicity, will be investigated in acute ischemic stroke patients receiving endovascular treatment to remove clot within 8 hours following stroke onset. Neu2000KWL will be administered before endovascular treatment.

NCT ID: NCT02831075 Recruiting - Diabetic Foot Clinical Trials

A Clinical Study Using Adipose-derived Stem Cells for Diabetic Foot

Start date: January 2015
Phase: Phase 1
Study type: Interventional

Stem cell therapy has been a new and effective therapy in recent years for diabetic foot.This study intends to establish an optimal clinical research program, and attempts to break the technical bottleneck in the stem cell therapy for treating diabetes related vascular complications.

NCT ID: NCT02830841 Completed - Clinical trials for Hepatic Ischemic and Reperfusion Injury

Liver Protection of RIPC in Pediatric Living Donor Liver Transplantation

RIPC-PLDT
Start date: January 2016
Phase: N/A
Study type: Interventional

Remote ischemic preconditioning(RIPC) is emerging as an promising therapeutic paradigm to combat the detrimental impact of ischemic and reperfusion injury. In liver transplantation, ischemic and reperfusion injury severely impacts the post-surgery liver function and patient outcome. This prospective, double blind, randomized clinical trial is aimed to test the protective effect of RIPC against hepatic ischemic and reperfusion injury in pediatric liver transplantation.

NCT ID: NCT02829398 Completed - Ischemia Clinical Trials

Determinants of Vasospasm and Delayed Ischemic Deficits in Aneurysmal Subarachnoid Hemorrhage

Start date: March 2008
Phase: N/A
Study type: Interventional

The risk of delayed cerebral ischemia (DCI) after subarachnoid hemorrhage (SAH) is associated with large cerebral artery vasospasm, but vasospasm is not a strong predictor for DCI. Assessment of cerebral autoregulation with transcranial Doppler (TCD) may improve the prediction of DCI. The aim of this prospective study was to assess the value of TCD-derived variables to be used alone or in combination for prediction of DCI

NCT ID: NCT02829151 Recruiting - Clinical trials for Critical Limb Ischemia

Comparison of Cilostazol-based Triple Antiplatelet Therapy Versus Dual Antiplatelet Therapy for Outcomes of below-the Knee Endovascular Intervention in Patients With Critical Limb Ischemia (TAP CLI Study)

Start date: February 21, 2017
Phase: Phase 4
Study type: Interventional

- Prospective, randomized, controlled, multi-center study - A total of 390 subjects with critical limb ischemia will be included according to inclusion and exclusion criteria. - Patients will be randomized in a 1:1:1 manner into triple antiplatelet therapy (TAP: aspirin, clopidogrel, cilostazol) group, dual antiplatelet therapy (DAP: aspirin, clopidogrel) A group, or DAP (aspirin, cilostazol) B group. - All patients will be treated with angioplasty for critical limb ischemia. - Patients will be followed clinically for 1 year after the procedure. - Ankle-brachial index and Image study follow-up (Duplex US or CT angiography) will be performed at 1 year.

NCT ID: NCT02828540 Completed - Ischemic Stroke Clinical Trials

Clinical Trial to Assess the Efficacy and to Evaluate Safety of HT047 in Patients With Acute Ischemic Stroke

Start date: August 4, 2016
Phase: Phase 2
Study type: Interventional

To assess the efficacy and to evaluate safety of HT047 in patients with acute ischemic stroke