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Reperfusion Injury clinical trials

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NCT ID: NCT02430116 Recruiting - Clinical trials for Ischemic Postconditioning

Mitochondrial Apoptotic Pathway Induced by Myocardial Ischemia-Reperfusion Injury in Human

Start date: June 2014
Phase: N/A
Study type: Interventional

Background: The cardiomyocytes apoptosis induced by ischemia-reperfusion(I/R) is one of the most important factors in the myocardial I/R injury(MIRI) undergoing cardiac valve replacement with cardiopulmonary bypass(CVRCPB),and Ischemic postconditioning (I-postC) can inhibit apoptosis of myocardial cells. Consequently, this study investigated the key genes and apoptosis signaling pathways of myocardium in patients undergoing CVRCPB. Methods: A total of 36 New York Heart Association class II or III patients with rheumatic heart disease (RHD) of both sexes, aged 21-59 years, who were scheduled for first cardiac valve replacement with CPB in the investigators' hospital from February 2014 to May 2015, were randomly divided into the following three groups (n=12 each): negative control group (NEG group); I/R group (POS group); and I-postC group (Treat group). In the Treat group, the procedure involved 5 min before opening the ascending aorta, aortic unclamping for 30 s, and cross-clamping for 30 s for three cycles, after which the ascending aorta was completely opened. The NEG and Treat groups were not treated. Thirty-six patients were assessed for arrhythmia and recovery of myocardial contractile function after reperfusion by electrocardiograms and degree of dependence on vasoactive drugs. The myocardial tissues of the right atrial appendage were obtained at 3 min before CPB was established in the NEG group, and at 45 min after opening the aorta in the POS and Treat groups. In all three groups, the myocardial tissues of the right atrial appendage were obtained and preserved at −80°C for further experiments. The right atrial appendage of three patients randomly selected in each group was fixed with RNA later (Qiagen, Hilden, Germany) in a centrifuge tube overnight at 4°C, and then preserved at −20°C for RNA extraction. Human 12×135K Gene Array profiling of mRNA expressions was undertaken in human cardiac muscle cells. Differentially expressed mRNAs verified by quantitative real-time RT-PCR were subjected to pathway analysis. The mRNA expressions of AIF, APAF1, CYCS, Bax, caspase-3, caspase-9, caspase-6, caspase-7, BCL2, BAG1, and PI3K were assessed by real-time RT-PCR and western blot analysis. The levels of myocardial apoptosis induced by I/R were investigated by TUNEL assays. The changes in MIRI induced by myocardial apoptosis were investigated by pathologic examination of the myocardium.

NCT ID: NCT02406950 Recruiting - Healthy Clinical Trials

Sitagliptin and Endothelial Dysfunction

Start date: February 2015
Phase: Phase 3
Study type: Interventional

Over the years, numbers of cardioprotective drugs have been evaluated to attenuate lethal ischemia-reperfusion (IR) injuries. There is little study whether sitagliptin protects against endothelial dysfunction induced by IR injury in humans.

NCT ID: NCT02299063 Recruiting - Clinical trials for Complication of Anesthesia

Dexmedetomidine Effect on Mitochondrial Function

Start date: November 2014
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that in addition to a known sympatholytic effect, intraoperative dexmedetomidine reduces adverse changes in mitochondrial function and structure attenuating ischaemia-reperfusion and end-organ injury for children with non cyanotic congenital heart defects having corrective heart surgery.

NCT ID: NCT02255006 Recruiting - Healthy Clinical Trials

Effect of Acupuncture to Endothelial Dysfunction Induced by Ischemia-reperfusion Injury

AURORAS
Start date: May 2014
Phase: N/A
Study type: Interventional

Some studies suggest that acupuncture improve flow mediated dilation (FMD) that represents endothelial function, but no study has investigated whether acupuncture protects against ischemia and reperfusion (IR)-induced endothelial dysfunction in humans. This is a prospective crossover study clinical trial. In the first crossover study, 20 healthy nonsmoking volunteers (25 to 40 years old) will be randomly assigned to acupuncture or control. Endothelium-dependent, FMD of the brachial artery will be measured before and after IR (15 minutes of ischemia at the level of the proximal upper arm followed by 15 minutes of reperfusion). Acupuncture will be performed from 10 minute after ischemia till the end time of reperfusion for 20 minutes. In the second single arm study, 16 volunteers are administered oral 5mg glibenclamide two hours before IR injury (n=8) or selective cox-2 inhibitor celecoxib 200mg twice a day for 5 days to know what mechanism is responsible for acupuncture effect on IR injury. FMD measurements and acupuncture intervention during IR injury are same as above mentioned.

NCT ID: NCT02001363 Recruiting - Clinical trials for Acute Myocardial Infarction

Efficacy Study of Glucagonlike Peptide-1 to Treat Reperfusion Injury

Start date: November 2013
Phase: N/A
Study type: Interventional

The investigators planned to research the cardioprotective effects of intravenous liraglutide on reperfusion injury.

NCT ID: NCT01957943 Recruiting - Clinical trials for Ischemia Re-perfusion Injury

Omega 3 Lipid Emulsions and Liver Transplantation

OTLT
Start date: May 2014
Phase: N/A
Study type: Interventional

The study Aims to investigate the possible beneficial impact of peri-operative or post-operative administration of Omega 3 enriched lipid emulsions on recipients for living donor liver transplantation.

NCT ID: NCT01834092 Recruiting - Surgery Clinical Trials

Study of the Glycocalyx in Abdominal Aortic Aneurysm

Endo_eAAA
Start date: April 2013
Phase: N/A
Study type: Interventional

The investigators want to measure the degradation of the endothelial glycocalyx before and after clamping the aorta, in patients operated for a abdominal aortic aneurism.

NCT ID: NCT01476969 Recruiting - Clinical trials for Ischemic Reperfusion Injury

Effect of Remote Ischemic Perconditioning on Acute Kidney Injury in Adult Valve Replace

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Remote Ischemic Perconditioning is effective on Acute kidney injury in adult valve replacement.

NCT ID: NCT01307371 Recruiting - Death Clinical Trials

Cell Therapy in Diabetic Patients With ST-Segment Elevation Myocardial Infarction(STEMI)

Start date: March 2007
Phase: Phase 1
Study type: Observational

The purpose of this study is to investigate the efficacy and mechanism of bone marrow mononuclear cells (BMMNC) transplantation for diabetic and non-diabetic patients with ST-segment elevation myocardial infarction (STEMI)who have undergone percutaneous coronary intervention (PCI).

NCT ID: NCT00989508 Recruiting - Cardiac Output, Low Clinical Trials

Myocardial Protection With Perhexiline in Left Ventricular Hypertrophy

HYPER
Start date: October 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Open-heart surgery causes injury of the heart muscle. Although this is usually mild, temporary and reversible, if it is severe it can endanger life and require additional high cost care. During surgery, techniques are used to protect the heart from injury, but these remain imperfect. Patients with a thickened wall of the heart (left ventricular hypertrophy) may be at greater risk. This study assesses the effect of facilitating sugar metabolism (a more efficient fuel) by the heart muscle using the drug Perhexiline given before the operation. This treatment has a sound experimental basis for improving outcome. If this improvement is confirmed surgical results could be improved. The investigators will be studying heart function, heart muscle energy stores and chemicals which quantify the amount of heart muscle injury. The investigators' hypothesis is that Perhexiline will improve the protection of the heart by decreasing damage that may occur during heart surgery.