Use of the VasoNova VPS System During PICC Placement in an Algorithm Confirmation Study Using Fluoroscopy

Vasonova

Status: Completed

Conditions: Any Condition Requiring a PICC Placement

Treatments: Device: VPS System

Study type: Interventional

Funder types: Industry

Identifiers

NCT01232933

TP-0120

Details and patient eligibility

About

Subjects meeting study requirements will be consented and have their PICC catheter placed using navigational technology and the tip placement confirmed with radiographic imaging.

Enrollment: 83 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult with a PICC placement order

Exclusion criteria

• Pregnant or nursing
• Abnormal ECG
• Anatomic irregularities or history that would prevent proper placement
• Subject does not consent to photography, release of data and x-ray confirmation
• Subject does not understand or is not willing to sign informed consent for the VPS implant procedure and data release

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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83 participants in 1 patient group

VPS System

Experimental group

Description:

Use of navigational VPS system to place catheter

Treatment:

Device: VPS System