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OpenTrials
Completed

NCT Number: NCT01807507

Clinical Verification Evaluation of VeinViewer® Device

Measure accuracy of vein width using VeinViewer®, compared against ultrasound imaging as a gold standard

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Christie Medical Holdings, Inc.

Kitchener, Ontario, N2G 4Y7, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be 18 years of age or older
  • Must be able to read and understand English to understand the consent letter

Exclusion criteria

  • Less than 18 years of age
  • Unable to read and understand English to understand the consent letter

Treatment and study plan

VeinViewer

Device

VeinViewer® is designed to improve vascular access treatment standards and provide the highest possible quality in volunteer care. The device is a non-invasive handheld electronic visual aid device designed to project an image of superficial, subcutaneous vascular structures on the surface of the skin. VeinViewer's primary purpose is to assist in vascular visualization for IV starts and blood draws.

Primary outcomes

  1. Device validation versus ultrasound

    Time frame: Immediately after assessment-Day 1

    The focus of this study is to understand the clinical effectiveness of the device.

Sponsors and collaborators

Lead sponsor

Christie Medical Holdings, Inc.

Industry

Registry information

Important dates

Study start
2011
Primary completion
2012
Study completion
2013
First posted
Mar 8, 2013
Registry last updated
Feb 3, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.