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Clinical Trial

An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema

NCT: NCT06035120 · RECRUITING

NCT IDNCT06035120
StatusRECRUITING
Start Date2024-02-22
Completion2028-03-31
SponsorPulmonx Corporation (INDUSTRY)
First posted
Last updated

Brief Summary

This is a prospective, open-label, multi-center, single-arm study planned to enroll 200 subjects with heterogeneous emphysema and collateral ventilation (CV) in the target lobe. Subjects will undergo instillation of AeriSeal Foam in the target lobe and subsequent assessment of CV status using Chartis Pulmonary Assessment System. Subjects with CV- status will then undergo placement of Zephyr Valve in the target lobe for bronchoscopic lung volume reduction (BLVR) and be followed for 24 months.

Frequently Asked Questions

What is An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema?

An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema is a clinical trial registered under NCT06035120. Current status: RECRUITING.

What is the status of NCT06035120?

The current status of NCT06035120 (An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema) is: RECRUITING.

When did An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema start?

An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema started on 2024-02-22.

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Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.