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Asthma clinical trials

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NCT ID: NCT00837967 Completed - Asthma Clinical Trials

Study to Investigate the Safety and Efficacy of High Dose of Symbicort® SMART in Japanese Patients

Start date: January 2009
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to compare the tolerability of Symbicort® Turbuhaler® 160/4.5 μg 10 inhalations with terbutaline Turbuhaler® 0.4 mg 10 inhalations for 3 days on top of Symbicort® Turbuhaler® 160/4.5 μg 1 inhalation twice a day (bid) in adult asthma patients.

NCT ID: NCT00837395 Terminated - Asthma Clinical Trials

Inflammatory Mediators and microRNA Analysis in Premenstrual Asthma

Start date: February 2009
Phase:
Study type: Observational

A small number of women with asthma have an increase in asthma symptoms during the premenstrual or menstrual period. This study is being done to investigate the possible causes of this premenstrual increase in asthma symptoms and to help asthma care providers identify those patients who may suffer from this condition.

NCT ID: NCT00836641 Completed - Asthma Clinical Trials

Safety and Immunogenicity of Sequential Pneumococcal Immunization in Preschool Asthmatics

PAPSI
Start date: October 2006
Phase: Phase 4
Study type: Interventional

Asthma is a major health problem in preschool children. Infections by pneumococci a the most frequent cause of airway infections, which tend to cause worsening of asthma. Vaccination against pneumococci is recommended by scientific boards and the medical community, in order to reduce the burden of disease. Data on the immunogenicity and safety of pneumococcal immunization in preschool asthmatics are scarce.

NCT ID: NCT00836368 Completed - Asthma Clinical Trials

In Vitro Basophil Responsiveness to Allergen Challenge After Gamma-tocopherol Supplementation in Allergic Asthmatics

Gammaphil
Start date: December 2008
Phase: Phase 1
Study type: Interventional

Purpose: This is a non-masked study with a primary endpoint of in vitro basophil activation by the allergen D. farinae, comparing basophil activation before and after seven days of supplementation. Secondary endpoints will include circulating antioxidant levels (tocopherols and metabolites), in vitro basophil activation to IgG anti-IgE and to N-formyl-methionyl-leucyl-phenylalanine (f-met-leu-phe), and monocyte and basophil responsiveness to in vitro endotoxin challenge. Participants: Twenty allergic asthmatic volunteers Procedures (methods): Volunteers will be given 1200 mg of a gamma tocopherol enriched supplement, a commercially available supplement form of vitamin E. Study participants will undergo assessment of general health, lung function assessment, symptom scoring, and epicutaneous skin test to allergens at baseline and after supplementation. Blood samples will be collected at baseline and after 7 days of gamma-T treatment.

NCT ID: NCT00835445 Completed - Asthma Clinical Trials

Biopsies and Polyps

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

Background: Nasal polyps are found in about 5% of asthmatic patients.A close link exists between the upper and lower airways and the concept of the "United Airways" has emerged mainly from studies on allergic rhinitis and asthma. However, other upper airway diseases, such as chronic sinusitis and nasal polyposis may influence lower airway diseases. As for nasal polyposis, eosinophils are the major effector cells in asthma and have been associated with a worsening of this condition. Aim: To compare normal nasal mucosa and nasal polyp biopsies from subjects with nasal polyposis with or without asthma. Hypothesis: Nasal polyps from asthmatic subjects show a more aggressive pro-inflammatory pattern of cytokine expression compared to nasal polyps from non asthmatic subjects, and therefore contribute to the development and severity of asthma.

NCT ID: NCT00835094 Completed - Asthma Clinical Trials

A Randomized Trial Assessing Once Daily Administration of Mometasone Furoate DPI in Asthmatics (Study P02177)

Start date: October 1, 2002
Phase: Phase 4
Study type: Interventional

This will be an open-label, randomized, parallel-group comparison of mometasone furoate dry powder inhaler (MF-DPI) 400 mcg once daily administered in the morning vs. the evening for 12 weeks in subjects with asthma.

NCT ID: NCT00832923 Completed - Asthma Clinical Trials

Improving Asthma Care Through Parental Empowerment

PEPAC
Start date: January 2009
Phase: N/A
Study type: Interventional

The overall aim of this study will be to perform a prospective randomized clinical trial of an enhanced version of the IMPACT DC intervention involving short-term case management to facilitate PCP follow-up appointments and to provide education for parents about how to communicate more effectively with their children's PCPs as a means (1) to improve the rate of utilization of primary care services for ongoing asthma care and (2) to enhance the self-efficacy of parents in their interactions with their children's provider regarding the child's asthma care needs in 150 parents of high risk children referred within the IMPACT DC Asthma Clinic.

NCT ID: NCT00832455 Completed - Asthma Clinical Trials

Pediatric ACTION3 (Identify, Treat, Control): Effectiveness of Adding Montelukast in Pediatric Subjects With Uncontrolled Asthma (0476-385)

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

a study to describe patient and physician satisfaction with montelukast therapy for the control of asthma used either as monotherapy or in combination with inhaled corticosteroids

NCT ID: NCT00831428 Completed - Asthma Clinical Trials

Screening Scottish Swimmers for Asthma and Rhinitis

CLE004
Start date: February 2009
Phase:
Study type: Observational

The Scottish National and District swimming teams will be screened for asthma and rhinitis using both mannitol challenge and sport-based exercise challenge.

NCT ID: NCT00831376 Completed - Asthma Clinical Trials

Trough Bronchoprotection Conferred by Levosalbutamol and Racemic Salbutamol

NAI009
Start date: January 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to compare the relative bronchoprotection (at trough) conferred by 2-week chronic dosing with levosalbutamol and racemic salbutamol in mild to moderate asthmatics. Patients will be preselected into two groups on the basis of their beta-2 adrenoreceptor polymorphisms. The investigators will evaluate if this has a differential effect on the bronchoprotection conferred by both formulations of salbutamol, as evidenced by a rebound in airway hyper-responsiveness, in order to determine whether any effect can be explained by the S enantiomer in the racemic formulation.