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NCT ID: NCT02194985 Completed - Fabry Disease Clinical Trials

Open-Label Extension Study of the Long-Term Effects of Migalastat HCL in Patients With Fabry Disease

Start date: March 14, 2015
Phase: Phase 3
Study type: Interventional

This is an open-label extension study intended to provide continued treatment with migalastat hydrochloride (HCl) for participants with Fabry disease who completed treatment of a previous migalastat HCl study. The study assessed the long-term safety and effectiveness of migalastat HCl.

NCT ID: NCT02194842 Active, not recruiting - Prostate Cancer Clinical Trials

Phase III Radium 223 mCRPC-PEACE III

PEACE III
Start date: October 2015
Phase: Phase 3
Study type: Interventional

The primary objective of the trial is to assess if upfront combination of enzalutamide and Ra223 improves radiological progression-free survival (rPFS1) compared to enzalutamide single agent in CRPC patients metastatic to bone

NCT ID: NCT02193035 Completed - Clinical trials for Aortic Valve Stenosis

Microparticles in Severe Aortic Stenosis

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

Microparticles are small cell fragments that can induce fat plaques, calcification and formation of thrombus. They can be released through multiple stimulations, but also the high flow of blood through partially obstructed aortic valves. In patients with severely obstructed aortic valves the investigators hypothesize that microparticles levels will be elevated and that they will go down after percutaneous treatment of the valves.

NCT ID: NCT02192268 Not yet recruiting - Pneumonia Clinical Trials

Assesment of the Effectiveness of High Frequency Oral Oscillation and Mask of PEP in Children With Pneumonia

PEP/HFOO
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The hypothesis of this study is that the physiologic effects of these (PEP/ HFOO) resources may have positive effects in this population of children with acute respiratory illness. Thinking about this physical and physiological issue and due to the absence of a study that has evaluated the effectiveness of these instruments in patients with pneumonia, the objective of this study is to evaluate the short-term effects OOAF and mask of EPAP in children hospitalized for community-acquired pneumonia.

NCT ID: NCT02192060 Completed - Dental Plaque Clinical Trials

Efficacy of a Triclosan Formulation to Control the Initial Subgingival Biofilm Formation

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

The aim of the study is to compare the effect of a suspension containing Triclosan in dynamic of the subgingival biofilm formation versus a Placebo suspension. The initial subgingival biofilm formation will be evaluated by means of Plaque Free Zone (PFZ).

NCT ID: NCT02189200 Completed - Clinical trials for Dietary Modification

Nutritional Counseling Associated With the Ingestion of Oat Bran in Hypercholesterolemic Subjects

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

Dyslipidemia is among the risk factors for cardiovascular diseases (CVD). Is's due to genetic and / or environmental factors such as inadequate dietary pattern. The occurrence of adverse events with statins, added to recent questions about their benefits on hard outcomes, opens a gap for the importance of seeking other forms of treatment of dyslipidemia, particularly in patients for secondary prevention. The consumption of oat bran, beta-glucan source of dietary fibers with supposed action in reducing the absorption of exogenous cholesterol and the endogenous synthesis of it, and source of avenanthramides, phytochemical compounds with alleged antioxidant in lipid membranes, can be effective strategy for secondary prevention of atherosclerotic disease.

NCT ID: NCT02189044 Completed - Conditions Clinical Trials

Pilates and Muscle Strength Respiratory

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

Introduction: Among the systems of the organism, it is believed that the respiratory system is the one which gets older faster due to the greater exposure to environmental pollutants over the years.The Pilates method has emerged as a form of fitness particularly providing general welfare to the individual. Objective: To evaluate the effects of Pilates' exercises on respiratory muscle strength in elderly women. Methods: The investigators have studied 07 women aged 60 and over, with preserved autonomy and cognitive skills. The Pulmonary Function Test (Spirometry) was performed using the Vitalograph® spirometer, model 8600. Respiratory muscle strength was obtained by technical measurements of maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP), through an analog Gerar manometer. The experiment lasted eleven (11) weeks. For comparative analysis of the data obtained in the evaluations, the investigators applied the paired t test and a significance level of 5%.

NCT ID: NCT02188940 Completed - Obesity Clinical Trials

Exercise Training to Lose Weight in Obese Asthmatics

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

Obese asthmatics have more severe symptoms, reduced lung function, poorer quality of life and a reduced response to inhaled corticosteroid medication compared to non-obese asthmatics. In addition, the impact of a weight-loss program on clinical control and psychological outcomes has been poorly demonstrated and the effect of exercise training remain unknown. The investigators aim to investigate the effect of exercise training in a weight-loss program on asthma clinical control (primary outcome), health factors related to quality of life and psychosocial symptoms (secondary outcomes) in obese patients with moderate-to-severe persistent asthma. Physical activity, inflammatory profiles and sleep disorders will also be evaluated. The investigators' hypothesis is that exercise as part of a weight-loss program is more effective to lose weight and improve asthma control, quality of life and psychosocial symptoms in obese asthmatics.

NCT ID: NCT02188355 Active, not recruiting - Clinical trials for Coronary Artery Disease

Prospective, Single-arm, Multi Centre Observations Ultimaster Des Registry

e-Ultimaster
Start date: June 2014
Phase:
Study type: Observational [Patient Registry]

The e-Ultimaster will further validate the safety and efficacy of Ultimaster DES system in unselected patients representing everyday clinical practice. Also the study will assess the impact of non-compliance with dual antiplatelet therapy, one month after stent implementation (frequently observed in every day clinical practice), on stent thrombosis.

NCT ID: NCT02188030 Recruiting - Clinical trials for Musculoskeletal Disorder of the Neck

Individual and Group Exercise Program for Industrial Workers With CANS: Randomized Controlled Trial

Exercise
Start date: June 2014
Phase: N/A
Study type: Interventional

This study is double-blinded RCT, whose aim is to assess if an individual exercise program is more effective to reduce complaints in neck, shoulders and arms that an group exercise program, in industrial workers. The participants will be randomly allocated to receive 12 treatment sessions of individual exercise training (IET) or in group exercise training (GET). Sessions will last 30 minutes and will be held twice a week for 12 weeks. Participants will also be encouraged to continue the use of medicines and other health care.