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Pathologic Processes clinical trials

View clinical trials related to Pathologic Processes.

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NCT ID: NCT01957345 Completed - Clinical trials for Platelet Dysfunction

Evaluation of a New Approach of the Diagnosis of Constitutional Functional Disorders of Platelets

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

The primary purpose of the study is to evaluate a standardized method of screening for platelet signalling defects in patients with constitutional disorders of platelet function of unknown origin. We hypothesize that such defects are under-diagnosed in patients, due to heavy workup and requirement of relatively large blood sample by conventional biochemical methods. We propose to analyse kinase signalling downstream platelet membrane receptors using multiplex flow cytometry quantification and fluorescent platelet barcoding.

NCT ID: NCT01926067 Completed - Clinical trials for Heart; Surgery, Heart, Functional Disturbance as Result

Monitoring of Cardiac Function With 3-axis Accelerometers

Start date: June 2012
Phase: N/A
Study type: Observational

Aim of the study: To validate accelerometers for continuous monitoring of global cardiac function during weaning from cardiopulmonary bypass (CPB) in cardiac surgery.

NCT ID: NCT01916408 Completed - Clinical trials for Cardiovascular Diseases

The Effects of Enzymes and Flavonoids on Inflammation and Coagulation After Marathon

Enzy-MagIC
Start date: August 2013
Phase: Phase 1
Study type: Interventional

The aim of the present study is to investigate changes in inflammatory status and incidence of infection after extreme aerobic physical stress (participation in a marathon). In addition, the impact of marathon running on the hemostasis and muscular state will be evaluated. Changes at the inflammatory, muscular, and rheological level will be related to ingestion of oral hydrolytic enzymes and bioflavonoids.

NCT ID: NCT01883713 Completed - Clinical trials for Other Functional Disturbances Following Cardiac Surgery

Study of Methemoglobin as a Biomarker of Tissue Hypoxia During Acute Hemodilution in Heart Surgery Patients

Start date: January 2013
Phase:
Study type: Observational

Acute and chronic anemia continue to be associated with increased mortality in a number of clinical settings, including cardiac and non-cardiac surgery. However, "We have no clinical measures that let us know of impending insufficient oxygenation as anemia progresses" (R.B. Weiskopf). The current proposal is based on experimental and clinical data which suggest that plasma methemoglobin (MetHb) may be a sensitive biomarker of tissue hypoxia and "anemic stress" in surgical patients. Hypothesis: Increased methemoglobin is a biomarker of tissue hypoxia during acute anemia. Primary Objective: To demonstrate a direct relationship between decreased Hb and increased MetHb in patients undergoing acute hemodilution on cardiopulmonary bypass (CPB).

NCT ID: NCT01627964 Completed - Clinical trials for Heart; Functional Disturbance

Motion Analysis and Assessment of Cardiac Function for Cardiac Images

Start date: August 2011
Phase: N/A
Study type: Observational

The study develops software for motion analysis and assessment of cardiac function for cardiac images. Cardiac catheterization ventriculography of several randomly selected patients were taken from our hospital's PACS system. The investigators remove the patient information on the images, and use the image for motion analysis and assessment.

NCT ID: NCT01513642 Completed - Clinical trials for Functional Disturbance Following Cardiac Surgery

Respiratory Physiotherapy After Cardiac Surgery

Start date: March 2009
Phase: N/A
Study type: Interventional

Although incentive spirometry is commonly used to avoid pulmonary complications in cardiac surgery patients, the breath-stacking technique has been proposed as an alternative to increase pulmonary volumes in the post-operative period. Objective: To compare inspiratory volume and electromyographic activity of respiratory muscles during breath stacking technique and incentive spirometry in patients undergoing cardiac surgery.

NCT ID: NCT01392807 Completed - Clinical trials for Hepatic; Functional Disturbance

Open-label Study to Assess the Pharmacokinetics of NKTR-118 in Patients With Impaired Hepatic Function

Start date: July 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the pharmacokinetics of NKTR-118 in patients with impaired hepatic function versus subjects with normal hepatic function.

NCT ID: NCT01310582 Completed - Vaginal Diseases Clinical Trials

Recovery Following Desflurane Versus Sevoflurane for Outpatient Urologic Surgery in Elderly Females

Start date: May 2011
Phase: Phase 4
Study type: Interventional

Numerous studies demonstrate that patients have improved immediate recovery characteristics following desflurane anesthesia compared to other volatile agents, including sevoflurane. There is limited evidence in the literature to suggest that patients undergoing sevoflurane, compared to desflurane anesthesia, may suffer from limitation in function and cognitive ability for an undetermined, but prolonged period of time following surgery. These differences are not explained pharmacokinetically and may be a result of a direct neurotoxic effect of sevoflurane. An unresolved question is the time required for the ability to return to complex tasks, such as driving, following anesthesia. Commonly, patients are advised not to drive or make important decisions for 24 hours following anesthesia, but this is not well-studied and proscribed on an empiric, rather than scientific, basis with very limited data available.This study will better define recovery characteristics and characterize the severity and duration of cognitive impairment following sevoflurane or desflurane anesthesia after brief outpatient urologic surgery in elderly females using tests of cognitive ability coupled with performance on a driving simulator and cognitive task tests to objectively measure not only testing performance, but also cognitive effort in performing these tests.

NCT ID: NCT01274754 Completed - Clinical trials for Functional Disturbances Following Cardiac Surgery

Neuroprotection With Erythromycin in Cardiac Surgery

Start date: November 2008
Phase: N/A
Study type: Observational

Neurological complications occur in open heart surgery with a frequency of 40% and they range from major neurological deficits (due to a stroke) to neurocognitive and behavioral disorders. This study aims to determine if erythromycin, a worldwide known antibiotic, protects the brain from damage when given in high doses before and during open heart surgery. The investigators consume that high dose of erythromycin will protect the brain with a pharmacological preconditioning against the global ischemia during the perioperative period of heart surgery.

NCT ID: NCT01141556 Completed - Self Efficacy Clinical Trials

Effects of High-dose Intravenous Selenium (Selenase®) in Adult Patients Subjected to Elective All-cause Heart Surgery

Start date: December 2010
Phase: Phase 3
Study type: Interventional

Selenoenzymes play a major role in protecting cells against lipid peroxidation and they are involved in the inflammatory response regulation. The degree of selenium deficiency correlates with disease severity and the incidence of mortality in critically ill patients. The aim of our study is to evaluate, if high dosis selenium supplementation (loading dose 4000 μg, daily dosage 1000 μg) results in a significant reduction of inflammation-induced organ dysfunction and length of ICU-stay in patients after heart surgery.