COPD Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with COPD or emphysema
- People who are at least 22 years old
- People with a body mass index (BMI) between 18 and 32
- People who are able to walk between 100 and 400 metres in a 6-minute walk test at the baseline exam
- People whose condition is stable and who are taking less than 10mg of prednisone (or an equivalent steroid) per day
- People who have not smoked — including tobacco, vaping, or marijuana — for at least 4 months before the screening interview
- People whose lung function test results (FEV1) fall between 15% and 50% of the expected value, and whose FEV1/FVC ratio is below 70%
- People whose CT scan shows that at least 25% of the lung tissue in each lung is damaged by emphysema
- People whose CT scan shows a particular pattern of emphysema (either evenly or unevenly spread), where at least one lung has a significant difference in damage between the upper and lower sections
- People whose lungs are significantly overinflated, as shown by a residual volume (RV) greater than 175% of the expected value
- People who score 2 or higher on the mMRC breathlessness scale, meaning their breathing difficulty noticeably affects daily activities
- People who have signed an informed consent form agreeing to take part
Who may not be able to join:
- People who are currently taking part in another clinical study involving surgery, a procedure, or medication
- People whose emphysema is caused by a condition called alpha-1 antitrypsin deficiency
- People who are women of childbearing potential
- People who have been hospitalised for COPD flare-ups more than twice in the year before screening
- People who have been hospitalised for a COPD flare-up within 6 weeks of the planned procedure
- People who have had two or more pneumonia episodes requiring hospitalisation in the past year
- People with significant ongoing mucus production or chronic bronchitis
- People who have had a heart attack, or have unstable or uncontrolled heart failure, within the 6 months before screening
- People who have previously had a lung transplant, lung volume reduction surgery, or any surgical or endoscopic procedure to reduce lung volume
- People with a significant airway condition called bronchiectasis
- People who are unable to safely stop taking blood thinners or anti-clotting medications for 7 days
- People with uncontrolled high blood pressure in the lungs, or a related heart condition called cor pulmonale, based on a recent heart ultrasound (confirm with trial site)
- People with a suspected lung tumour or lung cancer
- People whose CT scan shows large air pockets (bullae) taking up more than 30% of either lung, insufficient detail for the required analysis software, or all lung sections showing less than 25% disease damage
- People with a heart condition that the lead doctor (principal investigator) believes would make the procedure unsafe
- People whose total lung capacity (TLC) is below 100% of the expected value
- People whose lung gas transfer measurement (DLCO) is below 15% or above 50% of the expected value
- People with carbon dioxide levels in the blood above a certain threshold at screening (confirm with trial site)
- People with oxygen levels in the blood below a certain threshold while breathing room air at screening (confirm with trial site)
- People whose screening results indicate they may still be smoking (based on cotinine or carboxyhemoglobin levels)
- People who currently have a diagnosed substance use disorder
- People currently diagnosed with Major Depressive Disorder, Schizoaffective Disorder, Schizophrenia, Borderline Personality Disorder, or Bipolar Disorder
- People with any other condition that the investigating doctor believes would make participation unsafe or unsuitable
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Adnan Majid, MD, Beth Israel Deaconess Medical Center
Phone: 858-369-0000
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Absolute change in residual volume (RV)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.