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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02946229
Other study ID # 110.04-2016-GES-0005
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 26, 2016
Est. completion date December 6, 2016

Study information

Verified date March 2018
Source GE Healthcare
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is designed to collect data from a ultrasound device being used to evaluate feasibility of next generation algorithms for ultrasound data processing and does not test any health outcome.


Description:

The study is designed to collect data from a ultrasound device being used to evaluate feasibility of next generation algorithms for ultrasound data processing and does not test any health outcome. All eligible adults (aged 18 or older) will contribute case data from a convenience sample of maintenance hemodialysis population available at the study site and consistent with feasibility assessment of the technology. A relatively large feasibility population is used due to the need to test feasibility of multiple features across variations within this population.


Recruitment information / eligibility

Status Completed
Enrollment 142
Est. completion date December 6, 2016
Est. primary completion date December 6, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Are adults (aged 18 years of age or older) at the time of consent;

2. Are undergoing maintenance hemodialysis (MHD); AND

3. Are able and willing to provide written informed consent for participation

Exclusion Criteria:

1. Have anatomical characteristics or comorbid medical conditions that prevent completion of ultrasound scanning using the study device; OR

2. Are potentially put at additional risk by participating, in the opinion of the investigator.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Ultrasound scan
Collection of ultrasound data sets that include routine ultrasound data (eg, extravascular lung fluid, cardiac velocity time integral and inferior vena cava) on the commercial GE Vivid S70 Ultrasound System which are used to test feasibility of next generation ultrasound algorithms being developed to process these data types.

Locations

Country Name City State
United States Research By Design Evergreen Park Illinois

Sponsors (1)

Lead Sponsor Collaborator
GE Healthcare

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Diagnostic Ultrasound Exams Collection (number) of ultrasound images representative of sonographic findings routinely observed in the general imaging population. 1 day
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