A Prospective, Single Center, Randomized, Cross-over Clinical Trial to Assess the Safety and Effectiveness of the Veinplicity Venous Access Device
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Phlebotomy
- Sponsor
- Physeon GmbH
- Enrollment
- 200
- Primary Endpoint
- Rate of successful venous access on the first attempt.
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief 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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subject ≥ 18 years of age
- •Subject with history of failed venous access, venipuncture, or IV cannula placement
- •Subject agreed to required follow-up
- •Subject provided written, informed consent
Exclusion Criteria
- •Subject currently had compromised skin on either forearm or hand
- •Subject currently on any blood thinning medication other than 81mg of aspirin
- •Subject had been diagnosed with peripheral neuropathy, has had a complex fracture or surgery in the forearm, or has other condition that diminishes sensation in one or both arms, hands or fingers
- •Subject had a demand type pacemaker or defibrillator
- •Subject is female of child-bearing potential and had a positive urine pregnancy test
- •Subject had a history of seizure, convulsions or epilepsy
- •Subject had a known allergy to Epsom salts
- •Subject had any other condition that may affect the ability to complete study requirements
Outcomes
Primary Outcomes
Rate of successful venous access on the first attempt.
Time Frame: 7 days
Rate of adverse events associated with either the treatment or the venous access site.
Time Frame: 7 days
Secondary Outcomes
- User Perception of IV cannulation difficulty,(7 days)
- Subject Preception of IV cannulation pain(7 days)
- Subject Perception of Device stimulation(7 days)
- Time required to achieve successful IV cannula placement(time from initial puncture to successful IV cannulation)
- Number of attempts required to achieve successful IV cannula placement(over a 24 hour period)