A Study to Look at Day to Day Changes in Lung Function in COPD Subjects Taking Albuterol/Salbutamol and Ipratropium
| Status: | Completed |
|---|---|
| Conditions: | Chronic Obstructive Pulmonary Disease, Pulmonary |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 40 - Any |
| Updated: | 6/22/2018 |
| Start Date: | July 23, 2012 |
| End Date: | October 22, 2012 |
A 4-Week Randomized Cross-Over Study to Evaluate Daily Lung Function Following the Administration of Albuterol/Salbutamol and Ipratropium in Subjects With Chronic Obstructive Pulmonary Disease
The objective of this study is to assess the daily variation in bronchodilator response to an
inhaled short acting beta2-agonist (albuterol/salbutamol) and an inhaled short acting
anticholinergic (ipratropium) individually and when used in combination in subjects with
COPD.
inhaled short acting beta2-agonist (albuterol/salbutamol) and an inhaled short acting
anticholinergic (ipratropium) individually and when used in combination in subjects with
COPD.
Beta2-agonist and anticholinergics are a principle component of the pharmacologic management
of chronic obstructive pulmonary disease COPD. It has been demonstrated that the combination
of a short acting beta2-agonist and a short acting anticholinergic yields greater efficacy as
measured by FEV1 when compared with the response to the individual short acting
bronchodilators. However, daily bronchial response to these agents is poorly understood. It
is also poorly understood how the variation in magnitude of the response to the individual
agents and how the variation in response for one agent coincides with the variation in
response to the other agent. This study will seek to define the pattern of response of each
individual agent and the relationship between them. The study will also explore if the
combination of the two agents leads to less variation in response compared to the individual
agents. This is a randomized, open label, two period cross-over study. Eligible subjects will
be randomized to a sequence of either albuterol/salbutamol via metered-dose inhaler (MDI)
followed by ipratropium via MDI or the same dose of each bronchodilator given in the opposite
order. Each study period will consist of 10 clinic visits to be conducted over 10 to 14 days.
of chronic obstructive pulmonary disease COPD. It has been demonstrated that the combination
of a short acting beta2-agonist and a short acting anticholinergic yields greater efficacy as
measured by FEV1 when compared with the response to the individual short acting
bronchodilators. However, daily bronchial response to these agents is poorly understood. It
is also poorly understood how the variation in magnitude of the response to the individual
agents and how the variation in response for one agent coincides with the variation in
response to the other agent. This study will seek to define the pattern of response of each
individual agent and the relationship between them. The study will also explore if the
combination of the two agents leads to less variation in response compared to the individual
agents. This is a randomized, open label, two period cross-over study. Eligible subjects will
be randomized to a sequence of either albuterol/salbutamol via metered-dose inhaler (MDI)
followed by ipratropium via MDI or the same dose of each bronchodilator given in the opposite
order. Each study period will consist of 10 clinic visits to be conducted over 10 to 14 days.
Inclusion Criteria:
- Subjects must give their signed and dated written informed consent to participate.
- Subjects 40 years of age or older at Visit 1.
- Male or female subjects .
- An established clinical history of COPD.
- Current or former cigarette smokers with a history of cigarette smoking of >=10
pack-years at Visit 1.
- A post-albuterol/salbutamol FEV1/FVC ratio of <0.70 and a post-albuterol/salbutamol
FEV1 of >=30 and <= 70% of predicted normal values at Visit 1 calculated using NHANES
III reference equations .
Exclusion Criteria:
- A current diagnosis of asthma
- Women who are pregnant of lactating or are planning on becoming pregnant during the
study.
- Hospitalization for COPD or pneumonia within 12 weeks prior to Visit 1.
- Participation in pulmonary rehabilitation
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