NCT03109405

Assess Veinplicity Venous Access Device Safety and Effectiveness

A Prospective, Single Center, Randomized, Cross-over Clinical Trial to Assess the Safety and Effectiveness of the Veinplicity Venous Access Device

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 200 (actual)
• Sponsor: Physeon GmbH · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study was to examine the Veinplicity Device as an adjunctive IV cannulation tool in subjects with a history of difficult to access veins. The Veinplicity Device is intended to improve venous access rates in compromised patients by taking advantage of the increased circulation that results from provoked muscle stimulation. The study collected information about the device, intravenous access, user and patient perceptions for IV access, and any device or procedural complications or other adverse events. Device use was examined with patients in both a prone and upright position.

Conditions

• Phlebotomy

Interventions

Type	Name	Description
DEVICE	Stimulation-assisted venous access	Stimulation-assisted venous access
OTHER	20 guage cannula for IV, tourniquet optional	Standard IV cannulation using 20 ga needle, and use of tourniquet at discretion of nurse performing IV cannulation

Timeline

• Start date: 2015-06-01
• Primary completion: 2015-08-01
• Completion: 2015-08-01
• First posted: 2017-04-12
• Last updated: 2018-04-05