COPD Trial, Recruiting NCT06181357 Sponsor: University Hospital, Limoges Condition: COPD
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COPD Trial, Recruiting

NCT06181357
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 are able to give their informed consent and take part in the study
  • People aged between 35 and 80 years old at the time of signing the consent form
  • People who have emphysema (either evenly spread or unevenly spread across the lungs) confirmed on a CT scan taken within the last 6 months
  • People whose CT scan shows that at least 50% of the target lung lobe is destroyed
  • People who have stopped smoking for at least 3 months
  • People who experience significant breathlessness, scoring 2 or above on a standard breathlessness scale called the mMRC questionnaire
  • People whose breathing test results (after using a bronchodilator inhaler) fall within a specific range, showing moderately to severely reduced lung function (confirm with trial site for exact values)
  • People whose lung volume measurements (after using a bronchodilator inhaler) show that the lungs are significantly overinflated (confirm with trial site for exact values)
  • People who can walk at least 100 metres during a 6-minute walk test
  • People who are members of, or covered by, a French social security scheme

Who may not be able to join:

  • People whose main diagnosis is asthma
  • People who have had more than 3 flare-ups of their lung condition in the past year, or 2 or more that required a hospital stay
  • People who have had a heart attack or stroke in the 6 months before joining the trial
  • People who have had symptoms of heart failure in the 6 months before joining the trial
  • People whose chest CT scan shows certain abnormalities, such as a very large air pocket in the lung, a certain type of emphysema around the edges of the lung, a lung nodule larger than 0.8cm (unless it has been known and stable for more than a year), scarring of lung tissue, or abnormally widened airways
  • People whose lung blood flow scan shows that the lobe with the poorest blood flow is not the same lobe that has the most emphysema damage
  • People with evenly spread emphysema whose blood flow scan shows less than a 10% difference in blood flow between the lung being treated and the lobe being targeted
  • People whose blood oxygen level is very low or whose carbon dioxide level is very high, as measured by an arterial blood test
  • People whose heart ultrasound shows that the heart is not pumping effectively, or that the blood pressure in the lung arteries is too high
  • People who have previously had a lung removed, or have had lung surgery on the same side as the lobe being targeted in this trial
  • People who have previously had a collapsed lung (pneumothorax) on the same side as the lobe being targeted
  • People who have previously had an endoscopic lung volume reduction procedure
  • People who have been taking oral steroid tablets at a dose above 20mg per day within the 4 weeks before joining the trial
  • People with significant airway widening causing symptoms, or with certain bacterial or fungal infections in the airways
  • People with cancer that has spread to other parts of the body and who are currently being treated, or whose treatment ended less than 5 years ago
  • People who are pregnant or breastfeeding
  • People with a nickel allergy
  • People who are under legal guardianship or a court-appointed protection order
  • People who are currently taking part in another interventional clinical trial
  • People who have any other condition that, in the opinion of the trial doctor, could interfere with the study or affect their ability to participate fully — for example, untreated alcohol dependence, substance use, or difficulty attending regular follow-up appointments
  • People whose test results using a device called the Chartis system show that air is able to move between lung sections in a way that would affect the procedure (this is checked during the study process)

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 23 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: 05 55 05 68 92

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
University Hospital, Limoges
Registry
ClinicalTrials.gov
Start date
6 May 2024
Est. completion
6 June 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Pneumothorax rate

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: 23 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