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NCT ID: NCT01695421 Recruiting - Heart Failure Clinical Trials

The Effect of a Five Week Electrical Myostimulation Program in Chronic Diseases

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

Patients afflicted with Chronic Heart Failure (HF) typically do not maintain stable cardiac function for the remainder of their life and consequently require continuous medical management and intermittent hospital admissions. Several investigations have demonstrated that electrical muscle stimulation (EMS) produces positive physiologic and psychological adaptations in patients with HF. However not all the EMS modalities were been evaluated on this population or not even were tested based on present recognized gold standard clinical parameters after a short period of treatment. The primary aims of the proposed study is to: Determine the effect of a five week home based of three EMS modalities on prognostics markers, perceived quality of life, muscle force and electrical activity in subjects diagnosed with HF.

NCT ID: NCT01695122 Completed - Clinical trials for Head and Neck Cancer

Valproic Acid and Platinum-based Chemoradiation in Locally Advanced Head and Neck Squamous Cell Carcinoma

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate if the addition of valproic acid to standard platinum-based chemoradiation as definitive treatment of locally advanced Head and Neck squamous cell carcinoma can improve treatment outcomes, such as response rate.

NCT ID: NCT01694992 Recruiting - Stroke Clinical Trials

Very Early Rehabilitation in Acute Ischemic Stroke

VERIS-Brazil
Start date: March 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of a rehabilitation (physiotherapy) program in patients with acute ischemic stroke in Acute Vascular Unit and in general ward of Hospital de Clínicas de Porto Alegre, and to verify the degree of disability at fourteenth and third month, functional improvement at third month, the frequency of deaths and incidence of complications due to immobility and quantify the time spent in hospital.

NCT ID: NCT01693809 Active, not recruiting - Healthy Subjects Clinical Trials

The Effects of Caffeine on Vestibular Evoked Myogenic Potentials in Healthy Subjects

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The principal aim of this study is to evaluate the presence of changes in cervical vestibular evoked myogenic potentials (VEMPc) after acute intake of caffeine in healthy subjects. Secondarily, it wants to standardize normal values exam VEMPc in otorhinolaryngology service of the hospital.

NCT ID: NCT01693380 Completed - Influenza Clinical Trials

Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza

Xo_Gripe
Start date: May 2009
Phase: Phase 4
Study type: Interventional

Vaccinating schoolchildren against influenza would prevent the disease among non-vaccinated household members.

NCT ID: NCT01693172 Recruiting - Neoplasm Clinical Trials

Effect of an Early Mobilization Program on Outcomes After Major Cancer Surgery

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

The aim of this study is to evaluate the effect of an early postoperative physical rehabilitation program on the functional capacity and incidence of postoperative complications in patients undergoing major elective surgery for treatment of a neoplasm

NCT ID: NCT01693003 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Indacaterol Versus Tiotropium on Dynamic Hyperinflation in COPD

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Exercise intolerance is a major complain of patients with chronic obstructive pulmonary disease (COPD). Dynamic hyperinflation has been recognized as an important limiting factor responsible for the appearance of intolerable dyspnea during exercise. Regular treatment with long-acting bronchodilators promotes a more sustained reduction of hyperinflation and consequent symptom relief and increase in the patient's ability to overcome physical demands of daily life. Tiotropium bromide (TIO) is a new generation, long-acting anticholinergic bronchodilator that significantly improves lung function, reduces symptoms and improves exercise tolerance in patients with advanced COPD. Indacaterol is a new ultra-long duration (>24 h) β2-agonist, which promotes sustained dilation of the bronchi with a once-daily administration. Compared to tiotropium, indacaterol provides evidence that is as effective as tiotropium for bronchodilation, as well as other clinical outcomes such as dyspnea and state of health. However, comparative effects of indacaterol versus tiotropium with regard to outcomes in tolerance, dyspnea and dynamic lung hyperinflation during exercise is scarce. We hypothesized that indacaterol and TIO are not different in terms of exercise tolerance and its determinants (dynamic hyperinflation and dyspnea).

NCT ID: NCT01692717 Completed - Healthy Subjects Clinical Trials

Clinical Assessment Of Association Pharmacokinetics Atorvastatin + Losartana + Hydrochlorothiazide

Start date: February 28, 2013
Phase: Phase 1
Study type: Interventional

The objective of this clinical study, randomized, crossover is to evaluate the pharmacokinetic profile of the polypill (atorvastatin + lorsatana + hydrochlorothiazide) Laboratory Hypermarcas S / A, in relation to drugs Citalor ® (atovastatina - Pfizer) and Hyzaar ® (losartan + hydrochlorothiazide - Merck Sharp & Dohme) by comparing the serum concentration of analytes unchanged (AT, LS and HCTZ) in healthy subjects.

NCT ID: NCT01692548 Completed - ADHD Clinical Trials

Neurofeedback Intervention on the Development of ADHD in Children at Risk

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

Forty children considered at risk for ADHD (subclinical ADHD) will be randomized to either a neurofeedback intervention or waiting list.

NCT ID: NCT01692327 Completed - Obesity Clinical Trials

Study About High Fat Meal and Postprandial Lipemia

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

The hypothesis of the proposed project is that after a fat overload, the postprandial response is different in both groups, suggesting that the LPP will present the most significant damage in endothelial vasomotion in obese individuals, especially those with GI and T2DM. After the fat overload, we hypothesized that there will be a worsening of endothelial function and microvascular reactivity in OB/DM2 and OB group compared to C, but also find lower concentrations of incretins in OB/DM2 group compared to other groups. These hypotheses may be confirmed by techniques for evaluating microvascular function, the use of DFT skin for vasomotion evaluation and finally analysis of analytes through metabolic and cardiovascular read by Multiplex kit.