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Completed

NCT Number: NCT05567562

Anti-Platelets in Chronic Obstructive Pulmonary Disease

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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Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Brigham and Women's Hospital

Boston, Massachusetts, 02115, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

- COPD Cases:

  • COPD (FEV1/FVC < 0.7, FVC >= LLN), GOLD Stage I/II/III (FEV1 >= 40%)
  • Current or former smoker of at least 10 pack years

Inclusion criteria

- Controls:

  • Normal lung function (FEV1/FVC >= 0.7, FEV1 and FVC >= LLN)
  • Current or former smoker of at least 10 pack years

Exclusion criteria

  • Platelet count < 150,000/dL or self-report of a bleeding disorder;
  • Regular use of aspirin, clopidogrel or another antiplatelet medication;
  • Allergy to aspirin, clopidogrel, albuterol or iodine/IV contrast;
  • BMI > 35;
  • History of intracranial hemorrhage, severe GI bleed or other life-threatening bleed;
  • Use of blood thinner (e.g. warfarin, lovenox or novel oral anti-coagulants);
  • Continuous use of supplemental oxygen at home;
  • Regular use of an NSAID;
  • Daily use of oral steroids, theophylline, roflumilast, or loop diuretics;
  • History of organ transplant or autoimmune disease on systemic therapy (rheumatoid arthritis, lupus);
  • Use of a biologic medication with regular injections;
  • Other current lung disease (interstitial lung disease, idiopathic pulmonary fibrosis, asthma);
  • IV drug use within the last year;
  • History of lung surgery to remove part of the lung;
  • Known bullae or advanced destructive emphysema in more than 1/3 of the lungs;
  • Treatment for cancer (systemic therapy or surgical/radiation within the thorax) in the last 12 months;
  • Known diagnosis of pulmonary hypertension;
  • Known systolic heart failure (RV or LV EF < 40%);
  • Acute or chronic renal insufficiency (estimated glomerular filtration rate [GFR] <60 mL/min/1.73 m2 or self-report). GFR will be calculated using the CKD-EPI equation;
  • Current or planned pregnancy in the next year;
  • Regular marijuana smoking;
  • Exacerbation of respiratory symptoms within the previous 6 weeks, such as that requiring hospitalization, oral prednisone or antibiotics to control symptoms, or longer and not yet returned to baseline; and
  • Chest, abdominal or eye surgery, or a heart attack or stroke, within the last 3 months.

Treatment and study plan

dual anti-platelet therapy

Combination Product

dual anti-platelet therapy

Other names: aspirin 81mg EC tab, clopidogrel 75mg tab

Placebo

Drug

Placebo

Primary outcomes

  1. Pulmonary Microvascular Blood Volume, CV

    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

Secondary outcomes

  1. Pulmonary Microvascular Blood Volume

    Time frame: After 2 weeks of therapy

    Pulmonary microvascular blood volume on dual energy CT scan, comparing on dual antiplatelet therapy to placebo

  2. Oxygen Saturation

    Time frame: After 2 weeks of therapy

    Resting oxygen saturation

Other outcomes

  1. Small Vessel Fraction on CT

    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

  2. Percent Emphysema on CT

    Time frame: After 2 weeks of therapy

    Percent of lung below -950HU on non-contrast inspiratory CT

  3. Air Trapping on Expiratory CT

    Time frame: After 2 weeks of therapy

    Percentage of lung volume with attenuation <-856HU on expiratory CT

  4. Post-BD FEV1

    Time frame: After 2 weeks of therapy

    Forced expiratory volume in 1 second, post-bronchodilator

  5. Platelet Activation Measures

    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.

  6. FeNO

    Time frame: After 2 weeks of therapy

    Fraction of exhaled nitric oxide

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Official study title

Dual Anti-platelet Therapy in Chronic Obstructive Pulmonary Disease Study

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 5, 2022
Registry last updated
May 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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