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Study identifier: NCT06181357 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Trial Evaluating the Rate of Pneumothorax in Severe Emphysema Secondary to Endoscopic Volume Reduction With Two-stage ZEPHYR® Valves Versus Endoscopic Volume Reduction With One-stage ZEPHYR® Valves

Condition: COPD  ·  Sponsor: University Hospital, Limoges

PhaseNA
Planned participants244
Who can joinAll sexes, 35 Years to 80 Years
Healthy volunteersNo

About this study

Chronic obstructive pulmonary disease (COPD) affects 3.5 million people and is the third leading cause of death worldwide. Emphysema involves air retention in the lungs and is ultimately responsible for a major deterioration in the quality of life. Available drug treatments have moderate efficacy whereas surgical lung volume reduction can improve exercise capacity when offered to a very selected population but at the cost of significant morbidity and mortality. Endoscopic Lung Volume reduction with ZEPHYR® valves improves respiratory function at rest, exercise tolerance and quality of life in patients with little or no interlobar collateral ventilation. If this technique has therefore proven its effectiveness, it is not devoid of complications and is notably responsible for pneumothorax in 27% of cases. The management of this complication is clearly codified, ranging from patient monitoring to the removal of one or more valves. It is therefore a subject of major concern for multiple reasons: high incidence, lengthening of hospital stay, increase in the overall cost of care, potential loss of benefit for the patient in the event of permanent withdrawal. valves and above all a potentially fatal event. A new strategy for implanting ZEPHYR® valves in two stages has been developed in Limoges University Hospital. This innovative algorithm has been evaluated in several non-comparative single or multicenter studies. In those studies, pneumothorax' rate secondary to lung volume red…

This description comes directly from the study's public registry record.

Talk to the study team

Thomas EGENOD, MD  ·  05 55 05 68 92  ·  thomas.egenod@chu-limoges.fr

Eloise DOBBELS, MD  ·  eloise.dobbels@chu-limoges.fr

Always discuss trial participation with your own doctor first.

Locations (17)

CHU de BordeauxBordeaux, FranceRecruiting
CHU de BrestBrest, FranceRecruiting
Groupe Hospitalier Est - HCLBron, FranceNot Yet Recruiting
CHU de DijonDijon, FranceRecruiting
chu de GrenobleGrenoble, FranceRecruiting
CHU de LilleLille, FranceRecruiting
CHU de LimogesLimoges, FranceRecruiting
APHMMarseille, FranceRecruiting
Hopital Saint JosephMarseille, FranceRecruiting
CHU de NiceNice, FranceNot Yet Recruiting
APHPParis, FranceRecruiting
APHPParis, FranceNot Yet Recruiting

+ 5 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06181357