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Active clinical trials for "Asthma"

Results 3171-3180 of 3412

Comparison of Two Treatment Regimens in Asthmatic Patients

Asthma

The objective of the study was to compare in real life clinical practice two treatment regimens: inhaled glucocorticosteroid + salmeterol and inhaled glucocorticosteroid + montelukast.

Completed4 enrollment criteria

CARE - Quality Improvement in Asthma Secondary Prevention in Primary Care, Through Delegation of...

Asthma

Quality Improvement in Primary Care: delegation of check-ups to nurses in general practice

Completed2 enrollment criteria

Budesonide/Formoterol for Maintenance and Reliever Therapy Among Asthma Patients in Thailand

Asthma

The purpose of this study is to determine the incidence of misuse, i.e., over-use and under-use, of Budesonide/formoterol for maintenance and reliever therapy in usual-care setting.

Completed5 enrollment criteria

Asthma Control and Clinical Practice in Hungary 2009

Asthma Control Level

A prospective study led amongst pulmonologists. Patients asthma control level will be evaluated based on GINA guideline criteria. HRQoL measured by Visual analogue scale. Clinical practice: non controlled patients therapy assessed.

Completed4 enrollment criteria

Childhood Asthma and Schooling: The Truth Unveiled

Bronchial Asthma

Childhood Asthma and Schooling: The Truth Unveiled.

Completed3 enrollment criteria

Health2006 - an Observational Study of Cardiovascular Disease, Diabetes, Asthma and Allergy

Cardiovascular DiseaseType 2 Diabetes3 more

The aim is to assess the population prevalence of risk factors for different chronic diseases such as cardiovascular disease, type 2 diabetes, osteoporosis, asthma, and allergy. Risk factors include genetic and serologic biomarkers, questionnaire data on health and lifestyle. There are many hypotheses under study for each research field.

Completed3 enrollment criteria

Developing Asthma Interventions Using Community Based Research

Asthma

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.

Completed5 enrollment criteria

Pharmacogenetics of b2-Agonists in Asthma.

Asthma

This study will help to find out if having a certain genetic makeup influences how a person with asthma responds to salmeterol, one of the two drugs in Advair(R).

Completed13 enrollment criteria

Symbicort SMART (Symbicort Maintenance And Reliever Therapy)

Asthma

The purpose of this study is to investigate the extent of Symbicort use in patients prescribed Symbicort as maintenance and reliever therapy.

Completed2 enrollment criteria

REALL: A Retrospective Observational Study to Compare the Effectiveness and Cost-Effectiveness Between...

Asthma

This is a retrospective observational study utilising anonymised individual patient clinical and prescribing information routinely collected by UK General Practitioners (GPs). This information will be observed for two years, one year pre and one year post- "Index Prescription Date" (IPD). The IPD is the date when a patient was first switched to any option of the step-3 asthma treatment regimen. The one year before the IPD is the baseline period and will be reviewed for risk factors and confounding factors. The one year after the IPD is the outcome period and will be observed to see the outcomes of the new treatment.

Completed7 enrollment criteria
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