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NCT ID: NCT02308852 Suspended - Stroke Clinical Trials

Improving Bi-manual Activities in Stroke Patients With Application of Neuro-stimulation

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

Noninvasive brain stimulations (NIBS) will be used in healthy volunteers and in chronic stroke patients to improve bimanual activities and motor learning. Functional magnetic resonance imaging will be used to evaluate the mechanisms underlying bimanual activities and motor learning in healthy volunteers and in chronic stroke patients. A neuro-rehabilitation robot (REA2PLAN, AXINESIS, Louvain-la-Neuve, Belgium) will be used for motor learning.

NCT ID: NCT01743170 Suspended - Hypertension Clinical Trials

Telemonitoring of Hypertensive Patients

LAPTOHP
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The proportion of hypertensive patients achieving adequate blood pressure control meeting guideline targets remains low. Of hypertensive patients, only 50% are on antihypertensive medications. Of those on blood pressure lowering drugs, only 50% have their blood pressure controlled. The objectives of this study are: 1. To test the feasibility of telemonitoring of blood pressure in Flemish general practices. 2. To investigate in a randomized fashion whether telemonitoring enabled self-measurement of blood pressure leads to faster blood pressure control than self-measurement without the telemonitoring information. 3. The secondary endpoints include various blood pressure indexes, adverse effects, a simple assessment of quality of life, adherence, a log of technical problems, and cost effectiveness (EQ-5D-5L).

NCT ID: NCT01544699 Suspended - Stroke Clinical Trials

Impact of Non-invasive Brain Stimulation on Motor Recuperation

Start date: January 2012
Phase: N/A
Study type: Interventional

tDCS (transcranial direct current stimulation) will be used in chronic stroke patients to improve a variety of functions with superior or inferior limb.

NCT ID: NCT01519843 Suspended - Stroke Clinical Trials

Post Stroke Motor Learning

Start date: September 2010
Phase: N/A
Study type: Interventional

Noninvasive brain stimulations (NIBS) will be used in chronic stroke patients to improve motor learning. Functional magnetic resonance imaging will be used to evaluate the mechanisms underlying motor learning in healthy volunteers and in chronic stroke patients.

NCT ID: NCT01503073 Suspended - Stroke Clinical Trials

Noninvasive Brain Stimulation for Stroke

NIBSstroke
Start date: January 2008
Phase: N/A
Study type: Interventional

Noninvasive brain stimulations will be used in acute and chronic stroke patients to improve a variety of functions.

NCT ID: NCT01350674 Suspended - Tuberculosis Clinical Trials

Role of EBUS-TBNA in Diagnosing TB in Mediastinal/Hilar Lymph Nodes

Start date: December 2010
Phase: N/A
Study type: Interventional

This is an observational prospective study. Role of EBUS-TBNA (endobronchial ultrasound transbronchial needle aspiration) is evaluated to diagnose tuberculosis in mediastinal and/or hilar lymph nodes. The investigators analyse the specificity and sensibility of this technique to diagnose tuberculosis in mediastinal and/or hilar lymph nodes. Patients with mediastinal and/or hilar lymph nodes on X-ray or CT thorax where a tuberculosis is the most probable cause and who have no parenchymal lesions suspected for tuberculosis and without other lymph nodes that are more easily accessible or palpable will be included in this study.

NCT ID: NCT01345396 Suspended - Asthma Clinical Trials

Influence of an Asthma Education Programme on Asthma Control During Pregnancy

Start date: February 2010
Phase: N/A
Study type: Interventional

Asthma is the most frequent respiratory disease during pregnancy. In a third of cases, the level of asthma control can decrease during the pregnancy, especially between the 29th and the 36th week. The occurrence of such complications are linked with a high asthma severity level just before the conception and an history of respiratory complications in a previous pregnancy. Many reviews and recommendations claim that pregnant women with asthma should be included in an educational progamme. However, this is poorly studied. The purpose of this study is to observe if an educational programme given before the 20th weeks of gestation has an effect on asthma control until the end of gestation.

NCT ID: NCT01273779 Suspended - Severe Sepsis Clinical Trials

Safety and Efficacy of Talactoferrin Alfa in Patients With Severe Sepsis

OASIS
Start date: June 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Study will evaluate the safety and potential benefit of talactoferrin (recombinant human lactoferrin) as an addition to the standard care for severe sepsis.

NCT ID: NCT00787293 Suspended - Heart Failure Clinical Trials

Study of Safety and Efficacy of the Percutaneous Reduction of Mitral Valve Regurgitation in Heart Failure Patients

PTOLEMY-2
Start date: October 2008
Phase: Phase 2
Study type: Interventional

Improvement in heart failure with moderate to severe mitral regurgitation using a percutaneously delivered implantable device.

NCT ID: NCT00442299 Suspended - Clinical trials for Chronic Kidney Disease

Albumin Dialysis in End-Stage Renal Disease: Detoxification Capacity and Impact on Vascular Endothelial Function

Start date: April 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The uremic syndrome is mainly related to the retention of a host of compounds, due to altered glomerular filtration and other factors of renal dysfunction, e.g. tubular secretion. Uremic retention solutes are arbitrarily subdivided in three different categories according to their physicochemical characteristics and their subsequent behaviour during dialysis: (i) the small, water-soluble, non-protein bound compounds, (ii) the larger middle molecules, mainly peptides and (iii) the small protein-bound compounds (1). Although direct proof is lacking, several lines of evidence indicate that albumin is the most important carrier protein. Removal of protein bound uremic retention solutes is limited. The Prometheus® system fractionates blood into plasma and cellular components, using an albumin-permeable polysulfon filter (AlbuFlow®) with a specially designed sieving coefficient curve (1.0 for 2-microglobulin, >0.6 for albumin, <0.3 for IgG, <0.1 for fibrinogen and <0.01 for IgM). Due to the high sieving coefficient of the filter for large molecules (i.e. cut-off at about 250 kD) molecules up to the size of albumin (69 kD) easily pass from blood into the secondary circuit which is filled with isotonic sodium chloride solution, whereas larger molecules like fibrinogen (340 kD) cannot pass through the filter. In the secondary circuit the filtered plasma with the albumin-bound toxins flows through one or two adsorbers in a row with maximized adsorption capacity for putative liver toxins that are directly adsorbed (`fractionated plasma separation and adsorption' or FPSA). The purified plasma is then returned to the blood side of the albumin filter. In order to eliminate water-soluble toxins, blood thereafter undergoes hemodialysis using a conventional high-flux dialyser. We hypothesise that removal of protein bound uremic retention solutes can be improved by FPSA as compared to standard hemodialysis.