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NCT ID: NCT02321917 Completed - Inflammation Clinical Trials

Rheoparin-coated Tubing System for Minimized Extracorporeal Circulation (MECC)

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

In this study, the investigators would like to compare a heparin-coated tubing system for minimized extracorporeal circulation (MECC) with the conventional tubing system for MECC, which does not contain heparin coating. The MECC system has been used since 14 years in the investigators' hospital as an extracorporeal system to support circulation and provide oxygen to the tissues during coronary artery bypass grafting. Until today, the investigators performed more than 5000 MECC procedures in their department.

NCT ID: NCT02321852 Completed - Healthy Clinical Trials

Influence of Triflusal on Cognitive Functions in Healthy Subjects

Tribunal-Basel
Start date: January 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effects of the eNOS activating agent triflusal on episodic memory and cognitive functions in healthy participants.

NCT ID: NCT02321514 Active, not recruiting - Clinical trials for Mitral Valve Regurgitation

Expanded Clinical Study of the Tendyne Mitral Valve System

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

The purpose of this study is to evaluate the safety and performance of the Tendyne Mitral Valve System in the treatment of severe mitral regurgitation in patents with functional disability greater than or equal to NYHA Class II, who are not suitable candidates for surgical replacement with otherwise available devices. Follow-up evaluations will be conducted through 5 years post implantation.

NCT ID: NCT02321410 Completed - Clinical trials for Carotid Artery Disease

"In Vivo" Comparison in Human Carotid Atherosclerosis: Plaque Neovascularization

PLAVASC
Start date: February 2014
Phase: N/A
Study type: Interventional

Atherosclerosis may initiate early in life and takes years to progress. This contrasts to the abrupt coronary or cerebrovascular events occurring following the transition from a stable to an unstable atherosclerotic plaque. The causes of this discontinuity of the disease are complex and probably multiple. There is increasing evidence that, besides inflammation, neovascularisation of atherosclerotic plaques and intra-plaque hemorrhages play an important role in plaque instability ending-up frequently in acute thrombotic occlusion or distal embolisation of athero-thrombotic material associated with heart attack or stroke. Contrast-enhanced Ultrasound, is a bed-side non-invasive technique, which allows to enhance microvascular structures and to visualize the adventitia and intraplaque vascularization. Dynamic contrast-enhanced plaque MRI (DCE-MRI) which has also been evaluated for in vivo detection and quantification of plaque neovascularity. Together with the presence of a large lipid-rich core, thin fibrous cap, positive remodeling and active inflammatory infiltrate, plaque neovascularisation is considered a valid marker of high-risk (or vulnerable) plaque as demonstrated in histopathological studies using microvessel density. Aim of the study is to assess and validate the value of contrast enhanced ultrasound (CEUS), a bed-side technique, in detecting plaque neovascularisation and compare it with the quantitative assessment by DCE-MRI in carotis atherosclerosis. A group of 30 patients with asymptomatic carotid atherosclerosis (> 50% stenosis on Doppler ultrasound) will undergo Carotid Duplex ultrasounds and CEUS. High-resolution plaque MRI and DCE-MRI will be performed in the same patients and will be analyzed by two separate operators blinded to the results of the CEUS in order to detect the efficacy of CEUS when compared with in vivo DCE-MRI, as the standard of reference.

NCT ID: NCT02320955 Terminated - Brain Edema Clinical Trials

Swiss Prospective Autologous Bone Flap Resorption Study

SPARS
Start date: January 2015
Phase:
Study type: Observational

The complications after reimplantation of cryoconserved autologous bone flaps are reported inhomogeniously in the literature. Especially the incidence of bone flap resorption varies from 0% to about 30%. More recent retrospective studies seem to find higher resorption rates and thus suggest to implant artificial bone replacements from the start. The Swiss Prospective Autologous bone Resorption Study is the first propspective observational study designed to determine the true incidence of autologous bone resorption.

NCT ID: NCT02319590 Completed - Cardiac Failure Clinical Trials

Anti-Angiotensin-Receptor 1 (ATR1)-, Anti-Endothelin-Receptor A (ETRA)-Antibodies and T Cells in Cardiomyopathy

T-CARD
Start date: December 2014
Phase:
Study type: Observational

The study aims 1) to determine autoantibody titers against the AGTR1 receptor and against the ETA receptor, 2) to characterize cytokine expression profiles of heart-specific activated T cells in patients with systolic heart failure. Auto-antibody titers and specific cytokine expression profiles in heart-specific activated T cells will then be correlated with heart failure progression and outcome.

NCT ID: NCT02318823 Completed - Healthy Clinical Trials

Effects of Beer (Alcohol) on Social Cognition

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

The present study aims to evaluate effects of beer (alcohol) on social cognition.

NCT ID: NCT02318459 Completed - Muscle Weakness Clinical Trials

High Intensity Interval Training in Geriatrics

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

This is a pilot study for evaluating the feasibility of using High Intensity Interval Training in geriatric hospitalized patients compared to the standard current rehabilitation practice.

NCT ID: NCT02318251 Active, not recruiting - Clinical trials for Urinary Incontinence, Stress

Stress Urinary Incontinence Physiotherapy

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

The purpose of the present study is to compare two different physiotherapy programs regarding their effect on stress urinary incontinence.

NCT ID: NCT02316431 Completed - Neoplasm Staging Clinical Trials

Diagnostic Comparison of PET-magnetic Resonance and PET-CT in Patients With Oncologic Diseases

Workflow
Start date: December 2014
Phase: N/A
Study type: Observational

Diagnostic accuracy of PET/magnetic resonance and PET/CT will be compared concerning primary tumor, regional nodes, metastasis (TNM) staging and therapeutic influence. Workflow scenarios will be evaluated to create imaging protocols which are time efficient and diagnostically accurate.