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Asthma clinical trials

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NCT ID: NCT00734318 Completed - Asthma, Bronchial Clinical Trials

Study of FlutiForm® Versus Fluticasone Plus Formoterol in Adult Subjects With Severe Asthma

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The study compares the efficacy and safety of FlutiForm® vs Flixotide® plus Foradil® in the treatment of severe persisent asthma in adult subjects.

NCT ID: NCT00734292 Completed - Clinical trials for Mild to Moderate Asthma

Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of FlutiForm HFA pMDI in Adult Subjects With Mild to Moderate Asthma

Start date: September 2008
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to evaluate the early bronchodilating effect of SKP FlutiForm HFA pMDI compared to placebo.

NCT ID: NCT00733473 Completed - Asthma Clinical Trials

Nebulized Budesonide for Children Who Are Hospitalized for Acute Wheezing

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

The purpose of this study is to determine if adding nebulized budesonide to the systemic steroid for treatment of acute wheezing has any additive benefit in children who have hospitalized for acute wheezing.

NCT ID: NCT00733317 Completed - Asthma Clinical Trials

Budesonide for Emergency Treatment of Acute Wheezing in Children

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

The purpose of this study is to determine if adding nebulized budesonide to the systemic steroid for treatment of acute wheezing has any additive benefit in the emergency room.

NCT ID: NCT00733226 Completed - Asthma Clinical Trials

Effect of OM-85 BV on Wheezing Related Morbidity in Children With Recurrent Wheezing

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

The purpose of this study is to determine whether OM-85 BV (Broncho-Vaxom)has any effect on respiratory infections, infection related wheezing attacks, beta-2 agonist use, duration of attacks and effect on serum cytokine levels.

NCT ID: NCT00731575 Active, not recruiting - Asthma Clinical Trials

Viral Inception of Asthma: Prospective Study From Infancy to School-age

VINKU2
Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to study prospectively the early clinical and immunological events in children susceptible to rhinovirus induced early wheezing (i.e., recently found highest risk factor for recurrent wheezing/asthma) and the efficacy of systemic corticosteroid to modify these events. Up to 50% of children suffer from acute wheezing before school-age. The prevalence of childhood asthma is 5-7%. Although pediatric asthma is mainly allergic, the exacerbations are associated with respiratory viral infections in 95% of cases. The means to predict asthma from environmental factors have been limited mainly to sensitization to aeroallergens (3-fold risk), which start to develop usually at 2-3 years of age. VINKU 1-study (orig. VINKU-study) discovered simultaneously with two other groups, that early wheezing associated with rhinovirus, the "common cold" virus, is the strongest predictor of recurrent wheezing/asthma (up to 10-fold risky). Noteworthily, viral infections work as risk markers already during infancy, a lot earlier than the sensitization to aeroallergens. The investigators also found retrospectively that early wheezers affected by rhinovirus responded to 3 day course of oral prednisolone (inexpensive and widely available treatment): recurrent wheezing decreased by 50% during following 12 months and the difference appeared to continue. VINKU 5V-study is currently investigating the clinical history, prevalence of asthma and airway hyperreactivity of these same children at school-age. The mechanism of rhinovirus associated risk or why they respond to prednisolone are largely unknown. However, the susceptibility to rhinovirus infections is associated with atopy and therefore it is possible these children may have impaired anti-inflammatory (Treg) responses and more likely to wheeze with any pro-inflammatory response (Th1 or Th2). Moreover, they may not effectively clear viruses, because they can not limit rhinovirus to nose and it spreads to lower airways and causes wheezing. VINKU 2-study will prospectively investigate the immunological events in young first-time wheezers affected by rhinovirus, and prospectively study the clinical efficacy of systemic corticosteroid in them. Most likely these children will benefit from the drug in terms of less recurrent wheezing, the investigators will also explore immunological effects of the drug and their link to clinical efficacy. The results are expected to give basis for the prevention of asthma and for the development of new treatment strategies and they can be directly applied to clinical medicine.

NCT ID: NCT00728169 Completed - Asthma Clinical Trials

Developing Asthma Interventions Using Community Based Research

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to identify community resources and challenges in improving the health of community members with asthma. The primary goal of this project is to use Community-Based Participatory Research methodology to develop interventions aimed at improving asthma management in high-risk African American asthmatics. This "ground-up" longterm approach has never been tested before in asthmatics. The primary goal of this study will be accomplished with four specific aims: Aim 1. Conduct focus groups to identify barriers to asthma management in the target population. Aim 2. Use a community advisory board (CAB) consisting of participants selected from the various focus groups to gather information about solutions for the above barriers. Aim 3. Use the information from the CAB to develop an intervention to improve asthma self management behaviors in the target population. Aim 4. Refine the developed intervention based on feedback from focus groups conducted in Aim 1.

NCT ID: NCT00725582 Completed - Asthma Clinical Trials

Study Evaluating the Effect of IMA-026 on Allergen-Induced Late Asthma Response in Mild Asthma

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

The purpose of this study is to evaluate the effect of IMA-026, an antibody to IL-13, on airway hyperresponsiveness and airway inflammation in mild asthmatics. IMA-026 will be given as 2 injections under the skin 1 week apart at 2 mg/kg each dose. The study will include a screening period and a treatment period which includes doses on day 1 and day 8.

NCT ID: NCT00723021 Completed - Asthma Clinical Trials

PF-04191834 Single Dose Bronchodilatory Study In Asthma.

Start date: July 2008
Phase: Phase 2
Study type: Interventional

Study to determine the bronchodilatory effects of PF-04191834 compared with zileuton in patients with asthma

NCT ID: NCT00722657 Completed - Asthmatic Patients Clinical Trials

Social-Economics Profile of the Asthmatic Patients Attended at Nucleus of Integrated Medical Care

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

This study had a descriptive, retrospective, transversal character with quantitative approach, which aimed to delineate the social-economics profile of the asthmatic patients that used the health service available at the Care Nucleon Medical Integrate (NAMI)