A Comprehensive Look at Vascular Access NCT01638065

Updated 06/21/2024

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

Vascular Access

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

See also
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	Completed	`NCT02644941` - Comparison of the Human Acellular Vessel (HAV) With ePTFE Grafts as Conduits for Hemodialysis	Phase 3
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