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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01638065
Other study ID # CP1011
Secondary ID
Status Completed
Phase N/A
First received July 9, 2012
Last updated January 30, 2014
Start date May 2012
Est. completion date July 2013

Study information

Verified date January 2014
Source Christie Medical Holdings, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 196
Est. completion date July 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility 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:

- 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

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Good Samaritan Hospital Downers Grove Illinois
United States LA County Hospital Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
Christie Medical Holdings, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary endpoint will be total number of attempts for successful cannulation. 1 day No
Secondary Amount of time for successful venous access 1 day No
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