Symbicort Onset of Action 2

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-03-31

Study Completion Date

2003-08-31

Brief Summary

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The purpose of this study is to compare the early onset of effect of Symbicort compared to Advair Diskus and Ventolin in adults with asthma

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Detailed Description

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Conditions

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Asthma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Study Groups

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1

budesonide/formoterol

Group Type EXPERIMENTAL

budesonide/formoterol

Intervention Type DRUG

2

fluticasone/salmeterol

Group Type ACTIVE_COMPARATOR

fluticasone/salmeterol

Intervention Type DRUG

3

albuterol

Group Type ACTIVE_COMPARATOR

albuterol

Intervention Type DRUG

Interventions

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budesonide/formoterol

Intervention Type DRUG

fluticasone/salmeterol

Intervention Type DRUG

albuterol

Intervention Type DRUG

Other Intervention Names

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Symbicort Advair Diskus Ventolin

Eligibility Criteria

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Inclusion Criteria

* At least 18 years of age
* Diagnosis of asthma and baseline lung function test results as determined by the protocol
* Required and received inhaled corticosteroids within timeframe and doses specified in the protocol

Exclusion Criteria

* Severe asthma or asthma that is markedly effected by seasonal factors
* Has required and received non-inhaled corticosteroids within the previous 4 weeks, has sensitivity to drugs specified in the protocol or requires treatment with beta-blockers

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No