Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
NCT Number: NCT05567562
This is a 6 week crossover study in current and former smokers with and without COPD to evaluate whether 2 weeks of dual antiplatelet therapy (aspirin 81mg and clopidogrel 75mg) improves pulmonary perfusion (i.e. blood flow in the lungs measured on a contrast CT scan) compared to placebo.
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Notify Me50 year–80 year
All sexes
Interventional
Phase 2
Boston, Massachusetts, 02115, United States
This is a single-center Phase IIa randomized double-blind crossover study in smokers with and without chronic obstructive pulmonary disease (COPD) to test whether dual antiplatelet therapy (aspirin 81mg and clopidogrel 75mg) improves pulmonary perfusion (i.e. blood flow in the lungs) compared to placebo.
We will enroll 30 subjects (20 with COPD, 10 without) who will each take part for 6 weeks. Participants and researchers will be blinded, they will not know which medications they are on first. Each participant will be asked to take aspirin and clopidogrel together for 2 weeks and also matching placebos for 2 weeks, with a 2 week washout period in between. Pulmonary blood flow will be evaluated with a contrast-enhanced CT scan of the chest two times over the 6 week study.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- COPD Cases:
Inclusion criteria
- Controls:
Exclusion criteria
dual anti-platelet therapy
Other names: aspirin 81mg EC tab, clopidogrel 75mg tab
Placebo
Time frame: After 2 weeks of therapy
Coefficient of variation (CV) of pulmonary microvascular blood volume on dual energy CT scan, comparing on dual antiplatelet therapy to placebo
Time frame: After 2 weeks of therapy
Pulmonary microvascular blood volume on dual energy CT scan, comparing on dual antiplatelet therapy to placebo
Time frame: After 2 weeks of therapy
Resting oxygen saturation
Time frame: After 2 weeks of therapy
Small vessel volume (vessels <5mm2 in CSA) as a percent of total lung volume, measured on non-contrast inspiratory CT
Time frame: After 2 weeks of therapy
Percent of lung below -950HU on non-contrast inspiratory CT
Time frame: After 2 weeks of therapy
Percentage of lung volume with attenuation <-856HU on expiratory CT
Time frame: After 2 weeks of therapy
Forced expiratory volume in 1 second, post-bronchodilator
Time frame: After 2 weeks of therapy
Platelet activation measures by flow cytometry: circulating monocyte-platelet aggregates (unstimulated), activated GPIIb/IIIa receptor, unstimulated, and stimulated by low and high dose arachidonic acid and adenosine diphosphate, and P-selectin on the platelet surface, unstimulated, and stimulated by low and high dose arachidonic acid and adenosine diphosphate.
Time frame: After 2 weeks of therapy
Fraction of exhaled nitric oxide
Brigham and Women's Hospital
Other
Dual Anti-platelet Therapy in Chronic Obstructive Pulmonary Disease Study
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