Inclusion criteria | |
• A diagnosis of COPD confirmed by spirometry showing a post-bronchodilator value of FEV1/FVC < 70 and a history of tobacco smoking or occupational/environmental exposure to smoke, gas, or dust | |
• ≥40 years of age | |
• Sinus rhythm ≥50/min and < 120/min at inclusion | |
• Written informed consent | |
Exclusion criteria | |
• Known hypersensitivity to metoprolol or related derivatives | |
• AV block II or III unless treated with a pacemaker | |
• Sinus bradycardia (resting heart rate < 50/min) | |
• Sick sinus syndrome unless treated with a pacemaker | |
• Atrial fibrillation/flutter | |
• Clinical signs or previous diagnosis of heart failure, angina pectoris, myocardial infarction, cerebrovascular disease, or critical peripheral ischemia | |
• Systolic blood pressure < 90 mmHg | |
• Tachyarrhythmia other than sinus tachycardia | |
• Sinus tachycardia > 120/min | |
• Severe bronchial asthma | |
• Current beta-blocker treatment | |
• Inability to provide informed consent | |
• Age < 40 years | |
• Acute on-going exacerbation of COPD | |
• Previous randomization in the trial | |
• Pregnancy (confirmed by pregnancy test when appropriate) |