HomeTrialNCT04186546
🔬NCT04186546ACTIVE NOT RECRUITING

Zephyr Valve Registry (ZEVR)

Study Summary

The purpose of this Post-Approval Registry is to gather ongoing safety and effectiveness assessment of the Zephyr Valve treatment in a real-world setting.

Conditions
Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment150 participants
Primary Completion
Lead SponsorPulmonx Corporation
Data Retrieved2026-04-11 04:20:19.561435+00:00
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