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Sonic Window Study Evaluation Plan

NCT02137148 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2015-03-04

No results posted yet for this study

Summary

The goals of this study are as follows; evaluation of the products' readiness to market, ascertain initial reactions by target users, evaluate actual use in potential clinical settings and any difficulties encountered with product use and actual venous cannulation.

Conditions

  • Non-palpable Veins

Interventions

DEVICE

Use of Ultrasound to assist in needle placement

Use of the Sonic Window handheld Ultrasound device to assist in needle placement by providing a coronal image of the patient anatomy.

Sponsors & Collaborators

  • Analogic Corporation

    lead INDUSTRY

Principal Investigators

  • Arveh Shander, M.D. · EHMC

Eligibility

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

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2015-01-31
Completion
2015-01-31

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 NCT02137148 on ClinicalTrials.gov