Clinical Trials Logo

Asthma clinical trials

View clinical trials related to Asthma.

Filter by:

NCT ID: NCT00922350 Completed - Acute Asthma Clinical Trials

Heliox and Posture in Patients With Asthma

Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to verify that nebulization with bronchodilators associated with heliox gas (helium + oxygen) and the posture of a leaning forward truck is effective in patients with an asthma attack.

NCT ID: NCT00921401 Completed - Asthma Clinical Trials

Improving the Quality of Asthma Care Using the Internet

Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

It is important for people with asthma to become involved in their asthma care and management. This study will evaluate an interactive Web site that provides tailored feedback and information to asthma patients and encourages them to ask their doctor specific questions about their asthma care.

NCT ID: NCT00920959 Completed - Asthma Clinical Trials

Advair Pediatric Once-Daily

Start date: November 2001
Phase: Phase 3
Study type: Interventional

To demonstrate if once-daily dosing of ADVAIR 100/50 once-daily has superior efficacy and comparable safety compared with FP 100mcg once-daily in pediatric subjects 4 to 11 years of age with asthma.

NCT ID: NCT00920621 Active, not recruiting - Asthma Clinical Trials

Randomized Trial: Maternal Vitamin D Supplementation to Prevent Childhood Asthma (VDAART)

VDAART
Start date: September 2009
Phase: Phase 3
Study type: Interventional

Vitamin D supplementation given to pregnant women will prevent asthma in their offspring and children.

NCT ID: NCT00920543 Completed - Asthma Clinical Trials

GSK BHR Study (Sont)

Start date: February 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study was to determine whether asthma control and reduced bronchial hyperresponsiveness could be achieved and maintained at a lower dose of inhaled corticosteroids with ADVAIR DISKUS twice-daily or FP twice-daily in adult and adolescent subjects with persistent asthma

NCT ID: NCT00920127 Active, not recruiting - Asthma Clinical Trials

Treatment With AKL1 in Obstructive Airways Disease (The TAKL Study)

TAKL
Start date: June 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Obstructive airways disease is a very common condition. This condition includes patients with asthma, chronic obstructive pulmonary disease (COPD), emphysema or chronic bronchitis. Some patients with obstructive airways disease have problems with long term breathlessness, wheeze and cough with or without sputum production. Currently the researchers give treatments - usually inhalers - which are designed to open the airways and reduce the breathlessness and wheeze. Despite these available treatments many patients still have continuing symptoms. Anecdotal clinical evidence suggested that a herbal remedy (called AKL1) has beneficial effects in respiratory conditions, with patients diagnosed as having both asthma and COPD reporting reduced symptoms including breathlessness and cough and reduced frequency of attacks.The purpose of this study is to confirm whether AKL1 does indeed have a meaningful benefit to patients with obstructive airways disease. The researchers will mainly be measuring any effect of AKL by assessing any change in trial subjects' coughs, using a questionnaire, but the researchers will also looking at breathing tests, walking tests, blood and sputum tests.

NCT ID: NCT00918944 Completed - Asthma Clinical Trials

Electronic Health Record (EHR) Decision Support to Improve Outpatient Asthma Care

Start date: January 2006
Phase: N/A
Study type: Interventional

To determine whether an innovative clinical decision support system embedded in an existing electronic health record (EHR) will improve provider adherence to the existing National Asthma Education and Prevention Program (NAEPP) guidelines. 12 primary care pediatric practices at The Children's Hospital of Philadelphia(both urban and suburban sites) will be randomized to receive either a passive EHR (control sites) or an interactive decision support system (intervention sites).

NCT ID: NCT00917787 Completed - Asthma Clinical Trials

Analysis of Blood-based Biomarkers of Asthma

ABBA
Start date: June 2009
Phase:
Study type: Observational

The purpose of this study is to analyze markers of inflammation in blood and in induced sputum for the purpose of identifying molecular markers of specific asthma phenotypes. The investigators' specific interest is demonstrating that periostin levels are higher than normal in blood. The investigators already have solid preliminary data to support this hypothesis, and our goal here is to replicate preliminary findings and extend them by examining further the characteristics of the asthma subgroup with elevated periostin levels.

NCT ID: NCT00917410 Completed - Asthma Clinical Trials

Mobile Phone Text for Optimizing Asthma Treatment

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

The study aims at providing information on how the Short Message Service (SMS) tool influences self-management in asthma patients and to assess the resulting health related effect. A wide range of models and theories exist in the compliance area, such as technical models, communication models, cognitive models and self-management models and theories. The use of some of these theories and models will serve as theoretical and explanatory tools for studying how and why the SMS tool influences the patient's self-management. Objective: The objective of this study is to assess the health-related effects of a SMS compliance and monitoring system for optimized asthma treatment in a controlled trial setting.

NCT ID: NCT00917215 Completed - Asthma Clinical Trials

Effectiveness of Acupuncture for Asthma

Start date: September 2008
Phase: N/A
Study type: Interventional

What is the trend of changes in asthmatic patients' daily peak expiratory flow (PEF) variability, pulmonary function, and quality of life (QOL) with acupuncture treatment on specific acupoints (CV22 and bilateral LU5, ST40, BL13, EXB1) compared with minimal acupuncture treatment (sham control group) on non-acupoints, and no acupuncture treatment (waiting list control group)?