Clinical Verification Evaluation of VeinViewer® Device

Completed

• Conditions: Vein Width
• Interventions: Device: VeinViewer

• Registration Number: NCT01807507
• Lead Sponsor: Christie Medical Holdings, Inc.

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2011-10
• Primary Completion: 2012-01
• Study First Submitted: 2013-03-06
• Study First Submitted QC: 2013-03-07
• Study First Posted: 2013-03-08
• Study Completion: 2013-07
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-30
• Last Update Posted: 2014-02-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 400

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Healthy Volunteers	VeinViewer	-

Primary Outcome Measures

Name	Time	Method
Device validation versus ultrasound	Immediately after assessment-Day 1	The focus of this study is to understand the clinical effectiveness of the device.

Trial Locations

Locations (1)

Christie Medical Holdings, Inc.; 🇨🇦 Kitchener, Ontario, Canada