Breathe Easier With Tadalafil Therapy for Dyspnea in COPD-PH

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age35-89
SponsorVA Office of Research and Development

About this trial

The investigators will study whether the drug tadalafil improves shortness of breath in 126 Veterans with Chronic Obstructive Pulmonary Disease (COPD) and high blood pressure in the lungs. The investigators will also assess whether tadalafil improves quality of life, home daily physical activity, exercise endurance, the frequency of acute flares of COPD, blood pressure in the lungs, and lung function. Veterans who enroll in the trial will be allocated by chance to either active tadalafil or an inactive identical capsule (placebo). Neither the Veteran nor the investigator will know whether the Veteran is taking tadalafil or placebo. Veterans will be followed closely in clinic or by telephone at 1, 2, 3, 4, 5, and 6 months, with attention to side effects and safety. At 1,3, and 6 months the investigators will repeat the questionnaires and testing of blood pressures in the lung and lung function. The investigators anticipate that the results of this study will determine whether tadalafil improves shortness of breath when added to usual medications for COPD.

Eligibility criteria

Qualifiers

Outpatients with COPD, defined as airflow limitation with post-bronchodilator obstruction on baseline visit spirometry, identified by FEV1/FVC < 70% or < the lower limit of normal (5th percentile of a normal population based on Global Lung Function Initiative reference equations), OR any emphysema on chest CT noted in a clinical radiology report confirmed by study investigator review.

Main Pulmonary Artery/Ascending Aorta (PA/A) diameter > 0.90 on clinically available CT scans within 12 months OR

Main Pulmonary Artery diameter > 30.8mm on clinically available CT scans within 12 months OR

outpatient echocardiography done within 6 months of enrollment demonstrating PA sys > 34 mmHg OR

Disqualifiers

Group 1 (Idiopathic, heritable, drug- or toxin-induced, Pulmonary Arterial Hypertension associated with connective tissue disease, congenital heart disease)

Group 2 (left atrial hypertension)

Group 3 PH not attributable to COPD

Group 4 (chronic thromboembolic PH) or other forms of PH not associated with primary lung disease.

Trial design

Treatments tested in this trial

  • Tadalafil
  • Placebo

Treatment groups

126 Participants
are divided into 2 treatment groups

Sponsors and collaborators

VA Office of Research and Development

Lead sponsor

VA Boston Healthcare System

Collaborator

Atlanta VA Medical Center

Collaborator

VA Eastern Colorado Health Care System

Collaborator

VA Nebraska Western Iowa Health Care System

Collaborator