Safety and Feasibility Study of the Chartis System

Pulmonx Corporation18 enrolled

Overview

The purpose of this study is to evaluate the safety and feasibility of the Chartis System in measuring air flow and pressures in isolated lung compartments during bronchoscopy.

Study Type

INTERVENTIONAL

Allocation

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

Conditions

Bronchoscopy

Interventions

Chartis SystemDEVICE

Assessment of airway flow and pressure

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Scheduled to undergo clinically indicated routine diagnostic bronchoscopy Exclusion Criteria: * Hyperexcretive chronic bronchitis or excessive sputum secretion * Active pulmonary infection * FEV1 \<20% predicted * FVC \<50% predicted

Locations (1)

Thoraxklinik am Universitatsklinikum Heidelberg

Heidelberg, Germany

Outcomes

Primary Outcomes

Adverse events

Time frame: Until discharge or 24 hours post procedure

Secondary Outcomes

Technical success

Time frame: During procedure

Data from ClinicalTrials.gov

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