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| Sponsor: | Teva Global Respiratory Research LLC |
|---|---|
| Information provided by: | Teva Global Respiratory Research LLC |
| ClinicalTrials.gov Identifier: | NCT00054964 |
Purpose
This study is designed to examine the effectiveness of a breath-operated albuterol inhaler in asthma patients who have difficulty using their standard "press-and-breathe" inhaler.
| Condition | Intervention | Phase |
|---|---|---|
|
Asthma |
Drug: Albuterol |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | IXR-202-4-167 |
| Study First Received: | February 14, 2003 |
| Last Updated: | May 6, 2008 |
| ClinicalTrials.gov Identifier: | NCT00054964 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Respiratory System Agents Neurotransmitter Agents Bronchial Diseases Adrenergic Agents Molecular Mechanisms of Pharmacological Action Albuterol Physiological Effects of Drugs Reproductive Control Agents Adrenergic Agonists Hypersensitivity Lung Diseases, Obstructive Respiratory Tract Diseases Tocolytic Agents |
Therapeutic Uses Immune System Diseases Adrenergic beta-Agonists Asthma Anti-Asthmatic Agents Pharmacologic Actions Autonomic Agents Lung Diseases Hypersensitivity, Immediate Peripheral Nervous System Agents Bronchodilator Agents Respiratory Hypersensitivity |