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 aged between 40 and 75 years old
- People who have been diagnosed with COPD, with breathing test results showing a specific level of airflow limitation and reduced lung function (confirm specific test values with the trial site)
- People whose COPD symptoms score at a certain level on standard symptom questionnaires, indicating a meaningful impact on daily life (confirm with trial site)
- People who have not smoked for at least 2 months before joining and who agree not to smoke for the entire duration of the trial
- People who, if they recently completed a formal lung rehabilitation program, did so at least 3 months before joining; or, if currently in a maintenance program, who agree to continue it through their 12-month follow-up
- People who have been taking standard COPD medications (in line with recognised COPD treatment guidelines) for at least 12 months before joining
- People who have received a flu vaccine in the past 12 months, or who agree to get one during the trial and annually for its duration
- People whose blood oxygen level at rest meets the minimum required level at the time of screening (confirm with trial site)
- People who are willing and able to complete all required tests, check-ins, and a patient diary throughout the trial
- People who understand the purpose of the trial, agree to take part, and are able to sign a consent form
Who may not be able to join:
- People whose body weight relative to their height (BMI) is below 18 or above 35
- People who have been diagnosed with asthma (as defined by recognised asthma guidelines)
- People who have been diagnosed with another active lung disease other than COPD (for example, active tuberculosis)
- People with a medical history of a collapsed lung (pneumothorax)
- People with a known allergy or medical reason they cannot receive the medications used during bronchoscopy or general anaesthesia, where this cannot be managed medically
- People who have had a respiratory infection or a COPD flare-up in the 4 weeks before joining
- People who have been treated with radiation or chemotherapy for cancer within the past 2 years
- People who are taking more than 10 mg per day of prednisone (or an equivalent steroid medication) at the time of joining
- People who have used opioid medications within the 3 months before joining
- People with a known disorder affecting how the digestive system moves food, or who have had surgery on the stomach, food pipe (oesophagus), or pancreas
- People who have an implanted electronic device (such as a pacemaker)
- People who have previously had lung or chest surgery, or who plan to have such surgery during the trial (including lung removal, lung transplant, or certain airway procedures)
- People who have had a heart attack in the last 6 months, or who have certain serious heart conditions identified on heart tests or assessments (confirm specifics with trial site)
- People assessed as being at high risk of high blood pressure in the lungs (pulmonary hypertension), based on heart scan results showing pressure above a certain level
- People with a lung nodule or other growth considered at high risk of being cancerous
- People with a significant lung airway condition called bronchiectasis, where airway walls are thickened and the airways are widened, causing persistent cough, mucus production, and repeated bleeding
- People for whom the trial's procedure is not considered feasible by the investigating doctor — for example, due to the shape of the airways or the severity of certain lung changes seen on a chest scan
- People with a total symptom score of 18 or above on a specific digestive symptom questionnaire used in this trial (confirm with trial site)
- People with any other disease or condition that might prevent them from completing the trial, including a life expectancy of less than 1 year
- Women who could become pregnant, unless a pregnancy test before treatment is negative and they agree not to become pregnant during the trial
- People who have taken part in another clinical trial and received an experimental treatment within the 3 months before screening
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: Fengming Luo, M.D., West China Hospital
Phone: +8613916444591
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
Change of Forced expiratory volume in first second (FEV1) relative to baseline
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.