COPD Trial, Recruiting NCT07086339 Sponsor: Pulmair Medical, Inc. Condition: COPD
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COPD Trial, Recruiting

NCT07086339
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 signed an informed consent form agreeing to take part
  • People who have been diagnosed with COPD or emphysema
  • People who are at least 22 years old
  • People whose body mass index (a measure of height and weight) falls between 18 and 32
  • People who can walk between 100 and 400 metres in a 6-minute walk test
  • People whose COPD is currently stable and who are taking less than 10 mg of prednisone (or a similar medication) per day
  • People who have not smoked, vaped, or used marijuana or any other tobacco or nicotine products for at least 4 months before their screening interview
  • People whose lung function test (FEV1) result falls between 15% and 45% of the value expected for someone of their age and size
  • People whose ratio of two lung function measurements (FEV1/FVC) is below 70%, indicating airflow limitation
  • People whose CT scan shows that at least 25% of the tissue in each lung has been damaged by emphysema, as confirmed by a specialist imaging laboratory
  • People whose CT scan shows that emphysema is present throughout both lungs (either evenly or unevenly), with at least one lung showing a 15% or greater difference in damage between the upper and lower sections, as confirmed by a specialist imaging laboratory
  • People whose lungs hold significantly more air than normal after breathing out (residual volume greater than 175% of the expected value)
  • People who rate their breathlessness at level 2 or higher on a standard breathlessness scale (mMRC score)

Who may not be able to join:

  • People who are currently taking part in another clinical study that involves surgery, a medical procedure, or a medication treatment
  • People who have a condition called alpha-1 antitrypsin deficiency, a genetic disorder that can cause lung disease
  • People who are women of childbearing potential
  • People who have been hospitalised for COPD flare-ups (exacerbations) 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 been hospitalised for pneumonia two or more times in the year before screening
  • People who have significant ongoing mucus build-up or chronic bronchitis
  • People who have had a heart attack, or have unstable or poorly controlled heart failure, within the 6 months before screening
  • People who have previously had a lung transplant, lung volume reduction surgery, removal of lung tissue (bullectomy or lobectomy), or an endoscopic lung volume reduction procedure
  • People who have a significant airway condition called bronchiectasis
  • People who cannot safely stop taking blood thinners or platelet-inhibiting medications for 7 days
  • People who have uncontrolled high blood pressure in the lungs, or a related heart condition called cor pulmonale, based on a recent heart ultrasound
  • People who have a suspected or confirmed lung cancer or suspicious lung nodule
  • People whose recent high-resolution CT scan shows any of the following: large air pockets (bullae) taking up more than 30% of either lung; images that cannot be properly assessed using the required software; or all lobes of the lungs showing less than 25% emphysema damage (confirm with trial site)
  • People who have a heart condition that the treating doctor believes would make the procedure unsafe for them
  • People whose total lung capacity is below 100% of the expected value at screening
  • People whose lung gas transfer measurement (DLCO) is either below 15% or above 50% of the expected value at screening
  • People whose blood carbon dioxide level is above a certain threshold (PaCO2 greater than 50 mm Hg) at screening
  • People whose blood oxygen level while breathing normal room air is below a certain threshold (PaO2 less than 45 mm Hg) at screening
  • People whose screening tests show cotinine levels (a marker of nicotine exposure) or carbon monoxide levels in the blood above the specified limits, which may indicate recent smoking or vaping
  • People who currently have a diagnosed substance use disorder
  • People who currently have a diagnosis of Major Depressive Disorder, Schizoaffective Disorder, Schizophrenia, Borderline Personality Disorder, or Bipolar Disorder
  • People who have any other condition that the trial investigator 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 13 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

Phone: +1-858-369-0000

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
4 February 2026
Est. completion
1 August 2027

Where this trial is recruiting

🇫🇷 France 🇳🇱 Netherlands

Primary endpoints

Incidence of serious adverse events

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: 13 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