Percussion Device (PD) for Detection of Pneumothorax

Status Terminated

Clinical Trial Summary

This study aims to examine the safety and efficacy of the Percussion Device in detecting a pneumothorax in patients that have undergone thoracic surgery.

Clinical Trial Description

A prospective, non-randomized clinical feasibility cohort study. The purpose of this feasibility study is to collect preliminary performance and safety information for the Percussion Device (PD). Patients satisfying the inclusion criteria will be approached for study enrolment before their surgery in clinic. Following surgery and after the patient's chest tube has been removed, evaluation of the chest using the PD and ultrasound will be performed by two independent assessors (a nurse practitioner or resident on the Thoracic Surgery Team) prior to the post-removal CXR. Details of study procedure are details in section 2.8. The PD's performance metric will be compared against CXR results, which is considered the gold standard in diagnosing a pneumothorax. ;

Study Design

Related Conditions & MeSH terms

Pneumothorax

Clinical Trial Details

NCT number	NCT03272815
Study type	Interventional
Source	Lawson Health Research Institute
Contact
Status	Terminated
Phase	N/A
Start date	May 10, 2018
Completion date	November 1, 2019

View Details

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