CClinicalTrials.gg
CompletedNCT01638065Updated Feb 3, 2014

A Comprehensive Look at Vascular Access

An observational study in Vascular Access, sponsored by Christie Medical Holdings, Inc.. Completed at 2 sites in United States. Per ClinicalTrials.gov, last updated 2014-02-03.

Sponsored by Christie Medical Holdings, Inc. · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
196
Sex
All
01

Study summary

The objective of this study is to show VeinViewer® Vision is an effective vein visualization device for peripheral vascular access, pre-, during, and post access.

02

Conditions studied

  • Vascular Access

Keywords

  • vein identification
  • vascular access
03

In context

Lead sponsor

Christie Medical Holdings, Inc. is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients at a medical facility requiring IV access.

Inclusion criteria

  • Requires peripheral venous access
  • Intact skin on areas of assessment
  • Patient and/or parent or legal guardian is able to understand consent

Exclusion criteria

Exclusion Criteria:

  • No Intact skin
  • Patient is under anesthesia during peripheral venous access
  • Patient is not a suitable candidate, as determined by the discretion of the investigator
05

Study design

Time perspective
Prospective
Enrollment
196 participants (actual)

Groups and cohorts

  • Standard

    Standard IV Access without device

  • VeinViewer

    IV access with VeinViewer device

06

What researchers measure

Primary outcomes

  1. The primary endpoint will be total number of attempts for successful cannulation.

    Time frame: 1 day

Secondary outcomes

  1. Amount of time for successful venous access

    Time frame: 1 day

07

Study locations

2 sites
  • LA County Hospital
    Los Angeles, California 90033, United States
  • Good Samaritan Hospital
    Downers Grove, Illinois 60515, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01638065
Lead sponsor
Christie Medical Holdings, Inc.
Responsible party
Sponsor
First posted
Jul 11, 2012
Start date
May 2012
Primary completion
Mar 2013
Completion
Jul 2013
Last update
Feb 3, 2014

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion