Clinical Evaluation of the Next Generation Venue Ultrasound System, Components, and Accessories - Canada

GE Healthcare35 enrolled

Overview

The purpose of the study is to collect images data sets from clinical cases and periodic user feedback on the Next Generation Venue ultrasound system under clinical conditions. This is a medical device study designed as a clinical, open label, unblinded, non-randomized, prospective, feasibility research study.

Adult patients (aged \>18 years) will be enrolled as they present for emergency or immediate medical care, in facilities such as the intensive care unit (ICU), cardiac care unit (CCU), and/or other departments. Subjects may or may not have a clinical indication for ultrasound scanning as part of their regular medical care and will be required to meet the inclusion criteria and none of the exclusion criteria. Eligible subjects will undergo an ultrasound exam using the investigational ultrasound device. The exam type will be based on the subject's clinical condition. Users performing the scans will periodically be asked to provide feedback on User Survey forms prepared by the Sponsor. Image data sets from investigational exam will be stored electronically and de-identified data will be disclosed to the Sponsor.Results are for use in development and optimization of a next generation ultrasound system being developed by study Sponsor, GE Healthcare (GEHC) prior to future commercial release.

Study Type

INTERVENTIONAL

Allocation

Purpose

DEVICE_FEASIBILITY

Masking

NONE

Enrollment

Conditions

Ultrasound Use in Emergency/Medical Care

Interventions

Ultrasound examDEVICE

Eligible subjects will be positioned for their ultrasound exam, which will take a similar amount of time and be performed in a similar manner as standard of care ultrasound exams at the site. The type and duration of ultrasound exam will be based on the subject's clinical condition.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Adults (aged 18 years of age or older) at the time of consent; 2. Eligible to undergo ultrasound scanning per the site standard of care (with or without a clinical indication for scanning); AND 3. Able and willing to provide written informed consent for participation. Exclusion Criteria: 1. Are pregnant subjects; 2. Require procedures that cannot be readily completed using available investigational devices; OR 3. Require or are anticipated to require medical care where study participation could reasonably be expected to adversely impact patient care.

Locations (1)

Hopital Notre-Dame

Montreal, Quebec, Canada

Outcomes

Primary Outcomes

Obtain Image sets using Ultrasound Venue System

Number of representative image sets for subjects enrolled in study

Time frame: Two months

Periodic user feedback

Periodic user feedback data from device users.

Time frame: Two months

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.