Endobronchial Silicone Valve for Patients With Emphysema
Recruiting now · Not applicable
Conditions studied: Emphysema
In brief
The purpose of this research is to evaluate the efficacy and safety of endobronchial silicone valve in patients with severe emphysema.
Key facts
- Study ID
- NCT07097896
- Run by
- China-Japan Friendship Hospital
- People needed
- 147
- Starts
- 2025-07-08
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2026-07-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical and radiological evidence of emphysema
- Nonsmoking for 4 months prior to screening interview
- BMI less than 35 kg/m2
- Stable on current medication regimen
- Forced expiratory volume in one second (FEV1) between 15% and 45% of predicted value
- Residual Volume less than 175% predicted (determined by body plethysmography)
- Little or no collateral ventilation (CV-) as determined using the Chartis System
You may not qualify if…
- Had two or more hospitalizations over the last year for a COPD exacerbation
- Had two or more hospitalizations over the last year for pneumonia
- Had a prior lung transplant, lung volume reduction surgery, bullectomy or lobectomy
- Had a heart attack or congestive heart failure within the last 6 months
- Have heart arrhythmia
- Is alpha-1 antitrypsin deficient
Where it is running
- China-Japan Friendship Hospital — Beijing, Beijing Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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