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NCT ID: NCT01300117 Recruiting - Cardiac Surgery Clinical Trials

Influence of Extracorporeal Circulation During Cardiac Surgery on the Development of Postoperative Thrombotic Thrombocytopenic Purpura (TTP)

Start date: October 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether extracorporeal circulation during cardiac surgery has an influence on ADAMTS13-Activity.

NCT ID: NCT01299168 Recruiting - Clinical trials for Incorporate Molecular Diagnosis Into Diagnostic Standards

Diagnostic and Therapeutic Applications in Microarrays in Organ Transplantation

Start date: May 2011
Phase:
Study type: Observational

The current standard for biopsy-based diagnoses of dysfunction of kidney transplants is the Banff Classification which represents arbitrary international consensus. Recent data-driven approaches using molecular and conventional technologies indicate that mere consensus produces frequently incorrect diagnoses with potential harm to patients due to inappropriate treatment. To address this unmet need and improve diagnostics in the area of organ transplantation, the Alberta Transplant Applied Genomics Centre (ATAGC) has developed a new diagnostic system that combines the molecular and histopathological features of transplant biopsies, plus clinical and laboratory parameters, to create the first Integrated Diagnostic System. The present study will validate and refine this system in 500 prospectively unselected biopsies for clinical indications from American, Canadian and European centres in addition to 300 biopsies already collected. Due to a considerable interest and support from participating Centers, the study is further extended to 1500 prospective biopsies. Thus this is the extension of the INTERCOM study (INTERCOMEX). In addition to demonstrating the feasibility and value of this System in routine patient care and clinical trials, the study will develop and optimize a transparent and user-friendly reporting format to communicate this information to clinicians and obtain detailed feedback on how this system can best improve patient care.

NCT ID: NCT01294813 Recruiting - Bronchoscopy Clinical Trials

Bronchoscopy and Electric Impedance Tomography (EIT) Pilot Study

Broncho-EIT
Start date: January 2011
Phase: N/A
Study type: Interventional

Electrical Impedance Tomography (EIT)is a technique based on the injection of small currents and voltage measurements using electrodes on the skin surface generating cross-sectional images representing impedance change in a slice of the thorax. It is a radiation free, non-invasive and portable lung imaging technique. Impedance changes in lung ventilation are investigated in mechanically ventilated patients who routinely undergo bronchoscopy in intensive care medicine. Bronchoscopy is performed to suction secretions as well as to analyze the secretions to recognize inflammations and diseases. It is an essential intervention which causes changes in ventilation which remain for 1-2 hours. It is not completely investigated why these changes in ventilation remain for so long time and how they are distributed regionally. Therefore the purpose of this study is to investigate the change in pulmonary regional ventilation in patients who routinely undergo bronchoscopy to possibly generate ideas how to optimize the ventilation after bronchoscopy to optimize the patient´s treatment.

NCT ID: NCT01292759 Recruiting - Clinical trials for Surgical Procedure, Unspecified

Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters

Start date: July 2010
Phase: N/A
Study type: Observational

Cardiac output can be monitored using different invasive devices. Nexfin HD is a new, noninvasive device that uses model flow technology to measure stroke volume and thus computes cardiac output (CO). To evaluate this new device the investigators compared esophageal doppler CO to Nexfin HD CO in patients scheduled for elective abdominal surgery.

NCT ID: NCT01292278 Recruiting - Clinical trials for Subarachnoid Hemorrhage

Constitution of Cerebrospinal Fluid and Blood Database/Specimen in Acute Stage of Subarachnoid Hemorrhage (aSAH) Patients

Start date: January 2006
Phase: N/A
Study type: Observational

Neuropeptide Y (NPY) may play a major role in the pathophysiology of aneurysmal subarachnoid hemorrhage (aSAH). To investigate the correlation of NPY in cerebrospinal fluid (CSF) and blood (serum) and the neurological outcome in the acute stage of aSAH.

NCT ID: NCT01289795 Recruiting - Ischemic Stroke Clinical Trials

Endothelial Function and Progenitor Cells in Acute Ischemic Stroke

EPCAS
Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether levels of circulating endothelial progenitor cells (cEPC) are increased in the acute phase of ischemic stroke.

NCT ID: NCT01289652 Recruiting - HIV Clinical Trials

The Natural History and Treatment of Acute Hepatitis C Virus (HCV) in HIV-positive Individuals

PROBE-C
Start date: May 2011
Phase: N/A
Study type: Observational

The aim of the study is to investigate the epidemiology, natural history and treatment outcomes of acute hepatitis C (HCV) infection. Given the current pattern of case reporting, the cohort will be largely made up of human immunodeficiency virus (HIV)-positive patients, but HIV-negative patients with acute hepatitis C (AHC) will also be enrolled to enable comparisons to be made as appropriate and possible.

NCT ID: NCT01285479 Recruiting - Multiple Sclerosis Clinical Trials

The Gilenya Pregnancy Registry

Start date: October 15, 2011
Phase:
Study type: Observational [Patient Registry]

The purpose of the Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis (MS) is to continuously monitor, evaluate, and assess for major and minor teratogenic effects in the offspring of women exposed to fingolimod before (up to 8 weeks before last menstrual period (LMP)) and during pregnancy in routine clinical practice. The overall aim is to collect and evaluate data on maternal, fetal, and infant outcomes and compare it with reference populations.

NCT ID: NCT01281735 Recruiting - Clinical trials for Chronic Myeloid Leukemia

International Chronic Myeloid Leukemia Pediatric Study

ICMLPed
Start date: January 2011
Phase:
Study type: Observational

The purpose of the study is to describe and characterize CML in a large pediatric cohort of patients.

NCT ID: NCT01280019 Recruiting - Cardiac Surgery Clinical Trials

FRC Guided Therapy in Acute Respiratory Failure

Start date: October 2010
Phase: Phase 4
Study type: Interventional

In ventilated patients with acute respiratory failure endotracheal suctioning may lead to alveolar derecruitment, which can be monitored by means of functional residual capacity (FRC) measurements. Regional distribution of ventilation can be followed at bedside using electrical impedance tomography. The investigators hypothesize that a FRC guided recruitment strategy, aimed at restoring a baseline FRC value after open endotracheal suctioning, improves oxygenation and regional distribution of ventilation. In addition the investigators research the impact of such a strategy on the inflammatory response to mechanical ventilation.