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Asthma clinical trials

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NCT ID: NCT00686452 Recruiting - Asthma Clinical Trials

Airway Dysfunction and Remodelling in Athletes Following Swimming Training in Chlorinated Pools

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Start date: March 2007
Phase: N/A
Study type: Observational

Swimmers show the highest prevalence of asthma among elite athletes, certainly due to chlorine exposure. The consequences of a chronic exposure to chlorine compounds by swimmers and the mechanisms of asthme in this population are still poorly documented. Specific diagnostic criteria have been proposed by the International Olympic Committee - Medical Council (IOC-MC) and World anti-doping agency (WADA) to determine the presence of asthma in athletes. Using the more specific bronchial provocation tests, our aims are 1. to compare the prevalence of asthma in swimmers and control subjects 2. to analyze the Influence of chlorine exposure on bronchial inflammatory processes in swimmers versus control subjects 3. to study the time-course of changes in airway symptoms, responsiveness, inflammation and remodeling after cessation of training

NCT ID: NCT00672529 Recruiting - Asthma Clinical Trials

Orthomolecular Therapy and Asthma in Children

Start date: February 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is 1. To pilot the research methodology for a randomized trial on an orthomolecular treatment regime versus placebo as add-on therapy for children with asthma; 2. To obtain a preliminary estimate of the effectiveness of an orthomolecular treatment regime for allowing tapering of inhaled corticosteroids in clinically stable asthmatic children. The obtained estimate will allow sample size calculations for a full-scale randomized trial; and 3. To obtain preliminary information about the safety and tolerability of an orthomolecular treatment regime.

NCT ID: NCT00595491 Recruiting - Asthma Clinical Trials

Pilot Study to Identify the Mediators and Inflammatory Cell Surface Receptors Involved in Allergic Airway Inflammation

Start date: January 2008
Phase: Phase 1
Study type: Interventional

Asthma is a heterogeneous disorder in which multiple potential inflammatory pathways contribute to airway obstruction. The biological basis for airway inflammation is the subject of intensive investigation. This work is designed to identify airway factors that are responsible for recruiting cells and associate their airway presence with atopy and asthma.

NCT ID: NCT00576069 Recruiting - Asthma Clinical Trials

Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

Start date: October 25, 2007
Phase:
Study type: Observational

The purpose of this study is to evaluate the site and mechanisms responsible for expiratory airflow limitation in chronic, treated, non-smoking, stable asthmatics with moderate to severe persistent expiratory airflow obstruction. Treatment will include inhaled corticosteroids and long acting beta2agonists and long acting muscarinic antagonists. We are interested in determining whether the large and/or small airways are the predominant site of airflow limitation. We are also interested in determining whether intrinsic small airways obstruction and/or loss of lung elastic recoil is responsible for expiratory airflow limitation and to what extent may be attributed to loss of lung elastic recoil vs decreased airway conductance in peripheral airways. We are also interested to evaluate the role of varying doses of inhaled corticosteroids to suppress large and small airway inflammation using exhaled nitric oxide as surrogate markers of inflammation. For comparison purposes, spirometry and measurements of exhaled nitric oxide will also be obtained if possible during a naturally occurring exacerbation of asthma. High resolution thin section CT of the lung will also be obtained. Analysis will evaluate integrity of the lung parenchyma as to absence and or presence of emphysema and extent of emphysema using voxel quantification. We will also investigate optical coherence tomography to detect clinically unsuspected emphysema. We will also obtain autopsy material when available in asthmatics who expire. Will also measure serum periostin as a marker of inflammation by collaborating with Genetech in San Francisco.

NCT ID: NCT00500253 Recruiting - Asthma Clinical Trials

Assessment of Utility of Exhaled Nitric Oxide Measurement for Treatment Monitoring in Children With Asthma

Start date: February 2007
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess the utility of exhaled nitric oxide measurement (FeNO) in treatment monitoring in children with asthma. According to the aim of the study following assumptions are formulated: 1. Comparison of annual cumulative steroid dose, number of bronchodilator doses taken, number of asthma exacerbation, number of hospitalisation due to asthma, between group of children with asthma with FeNO monitored treatment (study group), and group of children with treatment monitored by GINA's grade of disease clinical control (control group) 2. Assessment of corelation of FeNO (ppb) with symptom score (points)and lung function (FEV1) 3. Comparison of values of non-specific bronchial hyperresponsiveness with methacholine (PC20M)between both study groups after 12. months of treatment.

NCT ID: NCT00496574 Recruiting - Asthma Clinical Trials

Evaluation of Efficacy of House Dust Mite Immunotherapy in Children With Bronchial Asthma

Start date: May 2006
Phase: Phase 4
Study type: Interventional

The aim of the study is to assess the effect of specific immunotherapy (SIT) to dust mites on clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function, bronchial hyperreactivity with methacholine, and presence and type of allergy after three years of SIT in children with asthma.

NCT ID: NCT00496561 Recruiting - Asthma Clinical Trials

Effect of Specific Immunotherapy to Dust Mites in Children With Asthma

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The aim of the study is to assess the effect of specific immunotherapy (SIT) to dust mites on clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function, chosen markers of inflammation, induction of regulatory lymphocytes, bronchial hyperreactivity with methacholine, and presence and type of allergy after two years of SIT in children with asthma.

NCT ID: NCT00494572 Recruiting - Asthma Clinical Trials

Montelukast With Status Asthmaticus, Ages 6-18

Start date: December 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if montelukast, in addition to standard treatment is helpful in treating patients ages 6-18 who are in the hospital because of status asthmaticus.

NCT ID: NCT00491790 Recruiting - Asthma Clinical Trials

Montelukast With Status Asthmaticus, Ages 2-5

Start date: December 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if montelukast, in addition to standard treatment is helpful in treating patients ages 2-5 who are in the hospital because of status asthmaticus.

NCT ID: NCT00425971 Recruiting - Asthma Clinical Trials

Safety Study of Anti-Asthma Agent BMEC-1217B

Start date: July 2008
Phase: Phase 1
Study type: Interventional

BMEC-1217B is an abbreviated version of an old Chinese formulation. The ratio of each component was adopted by the sponsor following the observation that BMEC-1217B prepared from this ratio resulted in best pharmacological profile and in vitro bioactivities. BMEC-1217B was studied for the pharmacological activity on the release of cysteinyl leukotrienes, IL-4 and TNF-alpha in vitro and the airway hyperreactivity. The result indicated that BMEC-1217B can inhibit the synthesis of several key pro-inflammatory mediators involved in the pathophysiology of allergic asthma and can also improve lung function in a mouse model of allergic asthma. The purpose of this study is to evaluate the safety and tolerability of increasing dose of BMEC-1217B when administered orally in healthy volunteers.