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Cinenses Lung Volume Reduction Reverser System First-in-man Study Treating Patients With Severe Emphysema

Emphysema Clinical Trial

Official title:
Evaluation of the Cinenses Lung Volume Reduction Reverser System in Treating Patients With Severe Emphysema

Clinical Trial Summary

The study is designed as a prospective, nonrandomized, exploratory, single center, first-in-man study. The objective of this study is to evaluate its safety and feasibility of the CinensesTM Lung Volume Reduction Reverser System in patients with severe emphysema. The study will also collect clinical data up to 6-month follow-up to explore its safety and effectiveness.

Clinical Trial Description

The study is designed as a prospective, nonrandomized, exploratory, single center, first-in-man study. The objective of this study is to evaluate its safety and feasibility of the CinensesTM Lung Volume Reduction Reverser System in patients with severe emphysema. The study will also collect clinical data up to 6-month follow-up to explore its safety and effectiveness. Study Population ：Patients with severe emphysema and have to meet all the inclusion and exclusion criteria. Sample Size： 15 subjects ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03685526
Study type Interventional
Source Lifetech Scientific (Shenzhen) Co., Ltd.
Contact
Status Active, not recruiting
Phase N/A
Start date May 6, 2019
Completion date August 1, 2022
View Details
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