Clinical Trials Logo

Asthma clinical trials

View clinical trials related to Asthma.

Filter by:

NCT ID: NCT00541255 Completed - Asthma Clinical Trials

A Long-Term Examination of Asthma From Childhood Through Adolescence

Start date: September 2007
Phase:
Study type: Observational

Asthma is a common disease that is often diagnosed in childhood. In some teenagers, asthma symptoms disappear and treatment can be stopped; however, for some of these people, asthma symptoms return in adulthood. This study will examine data collected over the lifetime of 18-year olds to identify factors that may increase a person's chance of having recurrent asthma as an adult.

NCT ID: NCT00540839 Withdrawn - Asthma, Bronchial Clinical Trials

A Study of Montelukast (MK-0476) Compared With Fluticasone in Pediatric Participants With Chronic Asthma (MK-0476-303)

Start date: November 2007
Phase: Phase 3
Study type: Interventional

A study to determine the effects of montelukast (MK-0476) on pediatric participants with chronic asthma compared with fluticasone. The primary hypotheses are that, over 24 weeks of treatment, montelukast will provide at least the same level of asthma control as inhaled fluticasone as measured by the percentage of days without asthma and that, over 24 weeks of treatment, daily administration of montelukast will be safe and well tolerated in children aged 6 months to 5 years with chronic asthma. This trial was stopped at a time before any participants had actually entered the trial. Based on input from regulatory agencies, it is not necessary to conduct this study; a separate ongoing study was sufficient for regulatory purposes.

NCT ID: NCT00538057 Completed - Asthma Clinical Trials

Comparing Two Respiratory Drugs When Used In Combination And Separately From A Novel Inhaler Device In Healthy Subjects

Start date: October 2, 2007
Phase: Phase 1
Study type: Interventional

A combination of the corticosteroid GW685698X and the long-acting ß2-agonist GW642444M is being developed for once daily administration for the maintenance treatment of asthma and COPD. GW642444M and GW685698X will be simultaneously co-administered from a single device and compared with GW642444M and GW685698X administered separately in order to determine whether co-administration affects the safety, tolerability, pharmacodynamic and/or pharmacokinetics of either compound.

NCT ID: NCT00536913 Completed - Asthma Clinical Trials

Evaluation of Safety and Efficacy of Symbicort® pMDI, With or Without Spacer, in Children (6-11 Years) With Asthma

Spacer
Start date: September 2007
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare Symbicort pMDI with and without spacer in terms of steroid potency, improvement of lung function and asthma symptoms in children with asthma (6-11 years).

NCT ID: NCT00536731 Completed - Bronchial Asthma Clinical Trials

Symbicort Rapihaler Therapeutic Equivalence Study

ESTHER
Start date: September 2007
Phase: Phase 3
Study type: Interventional

The purpose of the this study is to evaluate the efficacy and safety of 2 actuations Symbicort®pMDI® 40/2.25 μg twice daily compared with1 inhalation Symbicort Turbuhaler® 80/4.5 μg twice daily and 1 inhalation Pulmicort®Turbuhaler® 100 μg twice daily for 6 weeks.

NCT ID: NCT00536705 Completed - Asthma Clinical Trials

Effect of Montelukast on the Expression and Variation of TGF-β for Children With Mild Persistent Asthma

Start date: January 2009
Phase: N/A
Study type: Observational

The Objective of our research is to observe the effect of cysteinyl leukotriene receptor antagonist on the expression and variation of TGF-β1 levels and mRNA expression in children with mild persistent asthma in their plasma and T lymphocyte, to discuss the role of TGF-β1 in the pathogenesis of bronchial asthma in children and to evaluate the function of regulation of leukotriene receptor antagonist on asthma in children.

NCT ID: NCT00536042 Completed - Asthma Clinical Trials

Open-Label Trial of the Use of Minocycline in the Treatment of Asthma

Start date: October 1997
Phase: Phase 2
Study type: Interventional

The tetracycline minocycline has, in addition to its anti-infective properties, anti-inflammatory properties which may be of use in the treatment of asthma. This study evaluates the benefit of minocycline as add-on therapy for adults with asthma.

NCT ID: NCT00534625 Completed - Asthma Clinical Trials

Assessment of PFT, Safety, and PK of Zileuton Injection in Asthma Patients

Start date: September 2007
Phase: Phase 2
Study type: Interventional

A single intravenous injection of zileuton (150 or 300 mg) will be administered to patients with stable asthma. The goals will be to determine if zileuton i.v. can produce a rapid increase in FEV1/PEFR and when this effect can be seen. The safety of this route of administration of zileuton will also be studied. PK will be obtained in a population based method.

NCT ID: NCT00532922 Completed - Asthma Clinical Trials

A 3-Month Non-Interventional Study of Asthmatics Treatment With Symbicort® Turbuhaler®

Symb NIS
Start date: April 2007
Phase: Phase 4
Study type: Observational

The purpose of this study is to investigate real practices of treatment with Symbicort Turbuhaler for 3 months in asthma and patient compliance.

NCT ID: NCT00532831 Completed - Obesity Clinical Trials

Characterisation of Asthma in Obese Subjects

Start date: August 2005
Phase: N/A
Study type: Observational

Our hypothesis: Obese subjects with a physician's made diagnosis of asthma have a poorer asthma control than asthmatics with normal weight, less variability of peak expiratory flows (PEF) and bronchodilator response,increased induced sputum and systemic markers of inflammation and an increased prevalence of atopy. Obese subjects have an increased incidence of co-morbidities such as rhinosinusitis, gastroesophageal reflux and sleep apnea syndrome. This study aims to determine if, in comparison with asthmatics with a normal weight, paired for age and sex, obese subjects with asthma (all not using anti-inflammatory agents) show: - A more uncontrolled asthma, increased health care use and poorer quality of life - A reduced response to bronchodilators and diurnal variability of expiratory flows - More marked airway inflammation and evidences of a systemic inflammatory response - An increased prevalence of co-morbidities which can influence the report of respiratory symptoms or the severity of the disease, such as esophageal reflux symptoms, upper airway disease (rhinitis) and sleep apnea syndrome or other sleep disorder.