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Asthma clinical trials

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NCT ID: NCT00595114 Completed - Asthma Clinical Trials

Association Between Increased Oxidative Stress, Anti-Inflammatory Fatty Acid Formation, and Airway Infection in People With Asthma and Chronic Obstructive Pulmonary Disease

Start date: December 2007
Phase: Phase 0
Study type: Observational

Chronic obstructive pulmonary disease (COPD) and asthma are common respiratory diseases in which people experience long-term inflammation of the lungs. Exacerbations, or prolonged worsening of symptoms, of asthma and COPD are often life-threatening and can lead to frequent need for hospitalization. Even with the proper use of bronchodilators, corticosteroids, and other currently available medications, clinical responses among people with COPD and asthma are variable. There remains a significant unmet clinical need for new therapeutic approaches and insights, including the identification of biomarkers to accurately assess the presence of airway infection and intensity of airway inflammation. This study will investigate potential natural biological causes and new biomarkers for increased susceptibility to persistent airway infection in asthma and COPD.

NCT ID: NCT00590304 Completed - Asthma Clinical Trials

Asthma in the Delta Region of Arkansas: Characterization of Disease and Impact of Environmental Factors

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

The purpose of the study is to evaluate asthma and examine the homes of children with asthma living in rural areas of the state. This study is being done to give investigators more information about the presence of allergens and endotoxin in the homes of children with asthma living in the delta region of Arkansas.

NCT ID: NCT00590005 Completed - Asthma Clinical Trials

Redox Determinants of Severe Asthma (a Substudy of the Severe Asthma Research Program)

SARP
Start date: January 2003
Phase: N/A
Study type: Observational

Hypotheses: 1) Airway pH regulation is abnormal in severe asthma; 2) In severe asthma, there is formation of cytotoxic nitrogen oxides and loss of beneficial nitrogen oxides in the airways

NCT ID: NCT00589719 Completed - Asthma Clinical Trials

Asthma in the Delta Region of Arkansas (ADRA): Prevalence and Morbidity

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

The purpose of the study is to conduct a cross-sectional study to examine asthma prevalence and morbidity in a predominately minority, low-income population in rural Arkansas.

NCT ID: NCT00588406 Completed - Asthma Clinical Trials

Study of Budesonide as an Addition to Standard Therapy in Adult Asthmatics in the Emergency Room.

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

To determine whether adding nebulized inhaled steroids to the standard care of acutely ill ED patients with refractory acute asthma helps improve forced expiratory volume at one second (FEV1) and decrease the need for hospitalization.

NCT ID: NCT00587288 Completed - Asthma Clinical Trials

Efficacy and Safety Study of Reslizumab to Treat Poorly Controlled Asthma

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

The purpose of this study is to determine the effectiveness and safety of reslizumab (the drug under study) in the treatment of subjects with poorly controlled asthma.

NCT ID: NCT00585260 Completed - Asthma Clinical Trials

Mannitol Bronchoprovocation Challenge Ancillary Study/ACRN

Start date: December 2007
Phase: Early Phase 1
Study type: Interventional

This is an ancillary study conducted as part of the BASALT trial [NCT00495157]. The overall hypotheses are: 1) an indirect airway challenge procedure using mannitol can safely characterize asthma phenotypes, predict asthma control and exacerbations, predict responses to interventions, and perform more specifically than a direct methacholine challenge and; 2) PX27 pore function in whole blood correlates with measures of airway hyperresponsiveness induced by methacholine and/or mannitol challenges

NCT ID: NCT00585039 Completed - Asthma Clinical Trials

Albuterol Versus Xopenex in Treatment of Acute Asthma in the Emergency Department (ED)

Xopenex
Start date: September 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine in a large, double-blind, randomized, prospective pediatric clinical trial whether the use of continuous levalbuterol (Xopenex) in addition to standard emergency department treatment for acute asthma exacerbations will improve the Forced Expiratory Volume in 1 sec (FEV 1) compared to the use of continuous racemic albuterol. The secondary objective is to correlate clinical (hospitalization rates and clinical asthma scores) with plasma levels of (S)-albuterol.

NCT ID: NCT00584441 Completed - Asthma Clinical Trials

Menstrual Differences in Airway Inflammation in Asthma

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

Asthma is a chronic inflammatory lung disease characterized by airway hyper-responsiveness and reversible airway obstruction. Over the last decade, the prevalence of asthma is on the rise and it disproportionately affects more women than men. As much as 40% of women with asthma are known to have worsening of asthma symptoms and lung function prior to menstruation. This syndrome is being increasingly recognized as premenstrual asthma (PMA). The pathologic differences in female asthmatics with and without this syndrome are not known. The evidence regarding the role of sex hormones has been contradicting. We propose an observational cohort study to examine the changes in airway inflammation in women with asthma in relation to their menstrual cycle and their association with sex hormone levels. In addition we will include women on oral contraceptives to determine their effect on airway inflammation and asthma symptoms. We hypothesis that: - Women with premenstrual asthma will show increased indices of airway inflammation in various phases the monthly menstrual cycle. - In women with premenstrual asthma, a change in serum estradiol/progesterone ratio during the late luteal phase is associated with worsening of airway inflammation, air flow limitation and asthma symptoms. - The use of oral contraceptives is associated with suppression of the cyclical changes in airway inflammation due to lack of fluctuations in estradiol and progesterone levels. Recruited subjects will be asked to record asthma symptom scores, morning Peak Expiratory Flow Rate (m-PEFR) and rescue asthma medication (β2-agonist) used daily during the one month screening period to identify women with and without pre-menstrual asthma. Asthmatic women with regular menstrual cycles will be evaluated in their follicular phase (days 5-8) and luteal phase (days 21-24) and women on oral contraceptive pills (OCP) will be evaluated on days 9-12 of their OCP cycle and during the days 25-28, off of OCP consecutively for a 2-month period.

NCT ID: NCT00583986 Completed - Asthma Clinical Trials

Reliability of a Top Mount Actuation Indicator With Levalbuterol MDI in Adult and Pediatric Subjects With Asthma or COPD

Start date: September 2005
Phase: Phase 3
Study type: Interventional

This is a study to investigate the reliability, ruggedness and safety of the top mounted actuation indicator (TMAI) when used with Levalbuterol HFA MDI.