Utilizing a Near Infrared Vein Visualization Device To Increase Peripheral Intravenous Access Targets in Pediatric & Adult Patients (% Venous Options)

Christie Medical Holdings, Inc.1 site in 1 country300 target enrollmentJune 2011

ConditionsVeins

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Veins
Sponsor: Christie Medical Holdings, Inc.
Enrollment: 300
Locations: 1
Primary Endpoint: Number of Veins Identified with VeinViewer will be greater than those identified by sight or sight & palpation
Status: Completed
Last Updated: 14 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

VeinViewer® Vision will significantly increase the number of peripheral intravenous catheter access targets perceived by clinicians with experience in intravenous cannulation when compared to the number of access targets that these clinicians are able to visualize unaided or to palpate.

Registry

clinicaltrials.gov

Start Date

June 2011

End Date

December 2011

Last Updated

14 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

Christie Medical Holdings, Inc.

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Age 17 years of age or younger,
•Intact skin, without rash,irritation, scarring, open abrasion or other injury in these sites.
•Parent or guardian is English speaking
•Pediatric patients 8 years older will be asked to provide assent
•Participant does not have an acute or critical medical illness or injury requiring immediate evaluation and/or treatment.

Exclusion Criteria

•18 years of age or older
•No intact upper extremities
•Patient has had current or recent (within 6 months) venous access in the arm that will be evaluated.
•Acute or critical illness or injury requiring immediate or urgent evaluation and treatment.
•Inclusion Criteria:
•Age 18 years or older,
•At least one intact upper extremity (intact from the base knuckle to the shoulder)
•Intact skin on the dorsum of the hand, the ventral forearm, and antecubital fossa, without rash, irritation, scarring, open abrasion or other injury in these sites.
•Participant does not have an acute or critical medical illness or injury requiring immediate evaluation and/or treatment.
•Exclusion Criteria