Tolerability of Metoprolol-Succinate-ER and Carvedilol in COPD



Status:Completed
Conditions:Asthma, Asthma, Chronic Obstructive Pulmonary Disease, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:40 - Any
Updated:12/14/2017
Start Date:June 2004
End Date:June 2008

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Randomized Open-Label Crossover Trial Comparing Tolerability of a Cardioselective Beta-Blocker (Metoprolol-Succinate-ER) and a Non-Cardioselective Beta-Blocker (Carvedilol) in Patients With Chronic Obstructive Pulmonary Disease

Use of beta-blockers has proven beneficial in patients with hypertension, heart failure, and
in people who have suffered a heart attack. The use in patients who have Chronic Obstructive
Pulmonary Disease (COPD) and reactive airway disease, however, has been limited due to
possible side effects such as worsening of lung function or increasing airway spasms and
asthma attacks. The purpose of this study is to find out if patients with COPD can tolerate
being on a beta-blocker at doses recommended for the treatment of heart disease conditions.
This study also seeks to find out if a selective beta-1 receptor beta-blocker is better than
a non-selective beta-blocker in patients with mild to moderate COPD.


Inclusion Criteria:

- 40 years of age or older

- Mild to moderate COPD as defined by the American Thoracic Society

- Current treatment with a beta-blocker for either hypertension, myocardial infarction,
or congestive heart failure.

Exclusion Criteria:

- Recent (within 30 days) COPD exacerbation or requirement for oral steroid therapy
within the last 6 months

- Any history of ventilator support requirement for COPD

- Patients with asthma or reactive airway disease (RAD) defined as obstructive lung
disease with a >15% improvement in FEV1 with beta-agonist therapy

- Relative or absolute contraindication to beta-blocker therapy

- Exposure to any investigational drugs within the previous 30 days

- Patients with any concurrent disease or condition, which in the judgment of the
investigator would make the patient inappropriate for participation in the study were
excluded from this study
We found this trial at
1
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Los Angeles, California 90073
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Los Angeles, CA
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