COPD Trial, Recruiting NCT07119229 Sponsor: Pulmair Medical, Inc. Condition: COPD
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COPD Trial, Recruiting

NCT07119229
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Pulmair Medical, Inc.
Registry
ClinicalTrials.gov
Start date
25 March 2026
Est. completion
1 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Absolute change in residual volume (RV)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov