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Ischemia clinical trials

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NCT ID: NCT02649309 Recruiting - Clinical trials for Ischemic Reperfusion Injury

Single-cycle Remote Ischemic Preconditioning and Postconditioning (SCRIP) Trial

SCRIP
Start date: October 2015
Phase: N/A
Study type: Interventional

This trial is a 2 x 2 factorial design, double-blinded, randomized controlled trial to evaluate efficacy and safety of remote ischemic preconditioning and postconditioning in patient undergoing coronary angioplasty.

NCT ID: NCT02648958 Completed - Clinical trials for Arthroplasty, Replacement

Effect of Dexmedetomidine on Ischemia-Reperfusion Injury in Lower Extremity Operations

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

Ischemia reperfusion injury causes the release of free oxygen radicals. The selective alpha2-receptor agonist, dexmedetomidine, has an inhibitory effect on inflammatory responses during ischemic injury. The aim of this study is to evaluate the effect of dexmedetomidine on inflammatory responses during ischemia-reperfusion injury in skeletal muscle.

NCT ID: NCT02648230 Completed - Ischemia Clinical Trials

PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evaluation of FFR Measurements

PERFORM
Start date: December 2015
Phase: N/A
Study type: Interventional

The model by which physicians measure the lack of blood flow in the vessels that supply blood to the heart muscle is called Fractional Flow Reserve (FFR). FFR is the measurement of the pressure across the vessels that supply blood to the heart. These are known as the coronary arteries. This study involves comparing two FFR wires, the St. Jude Medical Pressure Wire (PW) and the ACIST Navvus Microcatheter (MC) to check the accuracy of the devices. FFR allows real-time estimation of the effects of a narrowed vessel, whereas standard angiography can underestimate or overestimate narrowing, because it only visualizes contrast (the different areas of color) inside a vessel.

NCT ID: NCT02646150 Completed - Ischemia Clinical Trials

Clinical Use of Magnetic Resonance Perfusion Imaging to Qualitatively Assess Adequate Distal Perfusion After Endovascular Revascularization in Critical Limb Ischemia

MR CLI
Start date: December 12, 2015
Phase:
Study type: Observational

This study evaluates the clinical effectiveness of Magnetic Resonance(MR) perfusion imaging to qualitatively assess adequate distal perfusion after endovascular revascularization in Critical Limb Ischemia

NCT ID: NCT02645240 Completed - Mesenteric Ischemia Clinical Trials

Predictive Factors of Intestinal Infraction in Acute Mesenteric Ischemia

Start date: October 2015
Phase: Phase 4
Study type: Interventional

The study aims to identify several factors that can accurately predict the incident of intestinal infraction in patients with mesenteric vascular occlusion or ischemia.

NCT ID: NCT02643784 Not yet recruiting - Ischemic Clinical Trials

Exploratory Study on the Effects of Early Rosuvastatin Treatment in Patients With Acute Ischemic Stroke

AIS
Start date: December 2015
Phase: Phase 4
Study type: Interventional

This is an exploratory, randomized, open-label, 2-arm, parallel-group study exploring the efficacy of rosuvastatin (20mg/day) in patients with acute ischemic stroke.

NCT ID: NCT02639806 Completed - Stroke Clinical Trials

General Anesthesia for Endovascular Thrombectomy; A Pilot Study.

Start date: January 2016
Phase:
Study type: Observational

This study evaluates the outcomes of stroke patients treated for intravascular thrombectomy, using either a local anesthetic with sedation, or a general anesthetic. Historical data will be used for those treated with the local anesthetic, and prospective data will be used for those treated with the general anesthetic.

NCT ID: NCT02637492 Completed - Clinical trials for Lower Limb Ischaemia

Development and Validation of a Clinical Prediction Rule for Lower Limb Critical Limb Ischaemia (PREDICCMI)

PREDICCMI
Start date: February 15, 2016
Phase:
Study type: Observational

Critical limb ischaemia (CLI) is the most serious stage of peripheral occlusive arterial disease (POAD). Despite progress in the revascularization procedures, half these patients experience amputation or death after one year. One issue is to identify these subjects because aggressive treatment is necessary in those cases, while in others (ie leg ulcer in a patient with POAD but no rest lower limb ischaemia), revascularization will not be necessary. Then it would be useful to develop a simple score to help the physician to improve diagnosis of CLI.

NCT ID: NCT02635464 Completed - Clinical trials for Chronic Ischemic Cardiomyopathy

Human Umbilical Cord-derived Mesenchymal Stem Cells With Injectable Collagen Scaffold Transplantation for Chronic Ischemic Cardiomyopathy

Start date: October 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The study is designed to assess the safety and efficacy of allogeneic human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) with injectable collagen scaffold transplanted into patients with chronic ischemic cardiomyopathy.

NCT ID: NCT02635347 Completed - Clinical trials for Carcinoma, Hepatocellular

Remote Ischemic Conditioning (RIC) in Recipients of Brain Death Donor Livers - A Feasibility and Safety Study

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

This study will assess the feasibility of lower limb-ischemia induced Remote Ischemic Conditioning (RIC) in the perioperative period before, during, and after Orthotopic Liver Transplantation (OLT). Remote ischemic conditioning will consist of 3 cycles of 5 minutes of lower limb ischemia induced via a mid-thigh pneumatic tourniquet, followed by 5 minutes of reperfusion. Interventions will take place after anesthesia induction but before surgery, at the completion of the procedure, and on the mornings of post-operative days 1-4.