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NCT05567562CompletedPhase 2

Anti-Platelets in Chronic Obstructive Pulmonary Disease

Dual Anti-platelet Therapy in Chronic Obstructive Pulmonary Disease Study

Source: ClinicalTrials.gov · Last updated 14 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
15 (actual)
First submitted
3 Oct 2022
Start date
27 Mar 2024
Primary completion date
28 Feb 2025
Lead sponsor
Brigham and Women's Hospital
Diseases
COPD
NCT number
NCT05567562

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 15
  • From 27 Mar 2024 to the primary completion date, 28 Feb 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Regular use of aspirin, clopidogrel or another antiplatelet medication;
  • Daily use of oral steroids, theophylline, roflumilast, or loop diuretics;
  • Use of a biologic medication with regular injections;
  • IV drug use within the last year;
  • 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

Other illness

  • Allergy to aspirin, clopidogrel, albuterol or iodine/IV contrast;
  • History of intracranial hemorrhage, severe GI bleed or other life-threatening bleed;
  • History of organ transplant or autoimmune disease on systemic therapy (rheumatoid arthritis, lupus);
  • Other current lung disease (interstitial lung disease, idiopathic pulmonary fibrosis, asthma);
  • History of lung surgery to remove part of the lung;
  • 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%);
  • Chest, abdominal or eye surgery, or a heart attack or stroke, within the last 3 months.

Lab values

  • Platelet count \< 150,000/dL or self-report of a bleeding disorder;
  • 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;

Other

  • BMI \> 35;
  • 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;
  • Known bullae or advanced destructive emphysema in more than 1/3 of the lungs;
  • Current or planned pregnancy in the next year;
  • Regular marijuana smoking;

Who the study is looking for

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

Age in the registry: 50 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brigham and Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.