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Asthma clinical trials

View clinical trials related to Asthma.

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NCT ID: NCT00380926 Completed - Allergic Asthma Clinical Trials

Fish Oil and Asthma in House Dust Mite Allergy

Start date: April 2004
Phase: Phase 2/Phase 3
Study type: Interventional

Native populations consuming high amounts of fish suffer less from allergic diseases. The purpose of this study is to determine whether polyunsaturated fatty acids (fish oil) might have a disease modifying influence on asthmatics sensitized to house dust mite.

NCT ID: NCT00380705 Completed - Asthma Clinical Trials

Quality of Life in Asthma and Rhinitis Allergic With Singulair (0476-365)

Start date: March 18, 2005
Phase: Phase 4
Study type: Interventional

Allow physicians not familiar with anti-leukotriene based therapy to test it

NCT ID: NCT00380484 Completed - Asthma Clinical Trials

Short- and Long Term Growth in Children With Asthma

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

The purpose of this study is to assess if treatment with budesonide 200 microgram per day affects short- or long term growth in children with asthma

NCT ID: NCT00380354 Completed - Asthma Clinical Trials

Study To Evaluate GSK256066 In Subjects With Mild Bronchial Asthma

Start date: September 2006
Phase: Phase 2
Study type: Interventional

This study will evaluate the efficacy and safety of GSK256066 in the treatment of subjects with mild bronchial asthma, using a number of clinical and biological markers of efficacy.

NCT ID: NCT00379288 Completed - Asthma Clinical Trials

Study of Mometasone Furoate/Formoterol Combination and Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Inhaled Glucocorticosteroids (P04139)

Start date: June 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety of mometasone furoate/formoterol (MF/F) metered dose inhaler (MDI) 200/10 mcg twice-a-day (BID) and MF/F MDI 400/10 mcg BID and two doses of fluticasone/salmeterol combination (F/SC) (250/50 mcg BID and 500/50 mcg BID) in subjects with persistent asthma who require maintenance treatment on inhaled glucocorticosteroids (ICS); evaluator-blind. In addition, the extrapulmonary effects on 24-hour plasma cortisol area under curve (AUC), of MF/F MDI 200/10 mcg BID, MF/F MDI 400/10 mcg BID, F/SC MDI 250/50 mcg BID, and F/SC MDI 500/50 mcg BID will be evaluated.

NCT ID: NCT00377663 Completed - Asthma Clinical Trials

Internet-Based Program to Improve Asthma Management in Children

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

Asthma is a respiratory condition that affects millions of children. It can be controlled, however, with the proper medications and treatment. AsthmaNet, an internet-based asthma management system, aims to improve the asthma care of children by providing their parents and doctors with appropriate tools and feedback related to asthma management. The purpose of this study is to evaluate the effectiveness of AsthmaNet at improving quality of care and controlling asthma symptoms in children.

NCT ID: NCT00377572 Completed - Asthma Clinical Trials

Inner-City Anti-IgE Therapy for Asthma

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

The purpose of this study is to find out if adding omalizumab to standard asthma treatment results in a safer, more effective, and longer lasting asthma treatment strategy than standard treatment alone, in inner-city children with mild to severe asthma.

NCT ID: NCT00377390 Completed - Asthma Clinical Trials

ICATA Asthma Mechanistic Study

Start date: October 2006
Phase: N/A
Study type: Observational

The purposes of this study are to determine the effects of omalizumab on cells involved in the allergic response, to evaluate predictors of response to omalizumab, and to determine whether response to omalizumab therapy is influenced by the environment. A subset of inner-city children and adolescents currently enrolled in Inner-City Anti-IgE Therapy for Asthma (a clinical trial of omalizumab) will be enrolled in this study.

NCT ID: NCT00377364 Completed - Asthma Clinical Trials

Acetaminophen (Tylenol) for Mood and Memory Changes Associated With Corticosteroid Therapy

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

Studies in humans and animals support that stress and/or elevations in corticosteroids lead to changes in hippocampal structure and functioning. This is important as patients with major depression frequently have elevated cortisol, and millions of patients receive prescription corticosteroids (e.g. prednisone). Both depression and corticosteroid therapy are associated with memory impairment and hippocampal atrophy. Our research uses corticosteroid-treated patients to explore interventions that might protect the brain from the effects of stress or corticosteroids. We propose to give 30 corticosteroid-treated asthma patients acetaminophen or placebo. Between group differences in mood, memory and other neurocognitive measures will serve as outcome measures.

NCT ID: NCT00373061 Completed - Asthma Clinical Trials

An Observational Study of the Use and Safety of Xolair® During Pregnancy

EXPECT
Start date: October 20, 2006
Phase: N/A
Study type: Observational

The Xolair® Pregnancy Registry is an observational study established by Genentech to obtain data on pregnancy outcomes in women who are exposed to Xolair®. Women exposed to at least one dose of Xolair® within 8 weeks prior to conception or at any time during their pregnancy will be followed to completion of their pregnancies. The evaluation of infants will be conducted at birth and at 6-month intervals until the infants are 12 months old. Follow-up of the infant will be extended until the infant is 18 months old, if the woman continues Xolair® treatment while breastfeeding.