Randomized 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

Status: Recruiting
Location: See all (15) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 reduction with endobronchial valves is rated between 4.5 and 12%. The efficacy of the treatment appears to be comparable with the data found in the trials evaluating in which the entire lobe was treated in one procedure. Moreover, despite two procedures, there does not seem to be any increased risk of occurrence of other complications. Finally, the systematic scheduling of a thoracic computed tomography between the two procedures showed that 26.6% of patients presented a reduction in volume greater than 350mL despite incomplete treatment. These data seem promising but no direct comparison with standard one-step treatment has ever been conducted so far.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 35
Maximum Age: 80
Healthy Volunteers: f
View:

⁃ Patient able to give informed consent and participate in the study

• Age ≥ 35 years old and ≤ 80 years old at the time of signing the consent

• Emphysema (homogeneous or heterogeneous) on a recent CT scan (\< 6 months). Heterogeneous emphysema defined by a difference of at least 15% destruction (threshold 910HU) between two adjacent lobes.

• Destruction ≥ 50% (threshold 910 HU) of the target lobe on the chest scanner

• Smoking quit for 3 months

• Dyspnea ≥ 2 according to the modified Medical Research Council (mMRC) questionnaire)

• Post-bronchodilator FEV between 15 and 50% theoretical

• Post-bronchodilator total lung capacity ≥ 100% theoretical and post-bronchodilator residual volume ≥ 175% theoretical

• Distance traveled during the TM6M ≥ 100m

• Member of or beneficiary of a social security scheme

Locations
Other Locations
France
CHU de Bordeaux
RECRUITING
Bordeaux
CHU de Brest
RECRUITING
Brest
CHU de Dijon
RECRUITING
Dijon
chu de Grenoble
RECRUITING
Grenoble
CHU de Lille
RECRUITING
Lille
CHU de Limoges
RECRUITING
Limoges
APHM
RECRUITING
Marseille
Hopital Saint Joseph
RECRUITING
Marseille
CHU de Nice
NOT_YET_RECRUITING
Nice
APHP
RECRUITING
Paris
APHP
NOT_YET_RECRUITING
Paris
CHU de Rouen
NOT_YET_RECRUITING
Rouen
chu de Strasbourg
RECRUITING
Strasbourg
Hopital Foch
RECRUITING
Suresnes
chu de Toulouse
RECRUITING
Toulouse
Contact Information
Primary
Thomas EGENOD, MD
thomas.egenod@chu-limoges.fr
05 55 05 68 92
Backup
Eloise DOBBELS, MD
eloise.dobbels@chu-limoges.fr
Time Frame
Start Date: 2024-05-06
Estimated Completion Date: 2027-06-06
Participants
Target number of participants: 244
Treatments
Experimental: two-stage ZEPHYR® valves
Sham_comparator: one-stage ZEPHYR® valves
Sponsors
Leads: University Hospital, Limoges

This content was sourced from clinicaltrials.gov