ABOUT THE TRIAL

Until now, COPD patients have had few options for managing their COPD exacerbation (flare-ups). As a participant in this study, you may see a decrease in the frequency and/or seriousness of your COPD exacerbations and help others with COPD in the future.

You may be eligible for this study if:

  • You have COPD and are taking regular (daily) medication to manage your COPD
  • Your COPD symptoms bother you often or much of the time
  • You are at least 40 and not older than 75 years old
  • You are not currently smoking (and will continue to not smoke)
  • You have been hospitalized or taken additional medications because of flare-ups in the past year

These are not the only eligibility requirements for this study and certain other criteria may exclude you.

See if you qualify.

How the study works

1. Eligibility Interview

Interested patients contact the study site to go through a list of eligibility requirements. If you are eligible, a member of the study team will invite you to come in for an initial screening examination.

2. Medical Screening

The study doctor or staff will review the study in detail, any known risks or benefits, your rights as a participant and other information you may need to make an informed decision. An initial medical screening will be performed and if you meet the initial eligibility requirements you may be scheduled for further evaluation. The healthcare provider will provide a full description of the study requirements.

3. The Procedure

The one-time non-surgical procedure involves passing a special catheter through a standard bronchoscope into the lungs. The catheter delivers a type of electrical energy called radiofrequency (RF) energy to the nerves located on the outside of the airways. Once the energy has been delivered, the catheter and bronchoscope are removed. The procedure takes about one hour. Learn more about the procedure.

4. Costs, Care and Follow-up Visits

All physician visits and medical visits are provided at no cost to you.

All trial participants will be under the care of a trial doctor, who is a lung specialist, for the entire time of the trial. Your status will be monitored for five years after the procedure. You will be able to contact the research team throughout this time period to address any questions or concerns.

For more information about clinical trials, the following websites may be useful:

Clinical Trials US National Institutes of Health
EU Clinical Trials Register
UK Clinical Trials Gateway
Canada Clinical Trials Database
World Health Organization International Clinical Trials Registry Platform

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