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Diagnostic Accuracy of Handheld vs Traditional Ultrasound

NCT05196776 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2023-11-01

Study results available
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Summary

Patients receiving a point-of-care ultrasound will be randomized into a portable, handheld device or a traditional cart-based ultrasound machine to compare diagnostic capability.

Conditions

  • Image, Body

Interventions

DEVICE

Portable, handheld point-of-care ultrasound device

The patient will have an ultrasound performed using a handheld, portable device.

DEVICE

Cart-based point-of-care ultrasound device

The patient will have an ultrasound performed using a traditional cart-based model.

Sponsors & Collaborators

  • Temple University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-01
Primary Completion
2022-03-01
Completion
2022-03-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05196776 on ClinicalTrials.gov