NCT04048863

Effect of B. Braun Peripheral Advantage Program on Complications, Indwell Time and First Stick Success of PIVC Therapy

Assessment of the Effect of B. Braun Peripheral Advantage Program on Complications, Indwell Time and First Stick Success of PIVC Therapy

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 44 (actual)
• Sponsor: B. Braun Medical Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Single sequence clinical study designed to evaluate the effectiveness of B. Braun PA on improved clinical outcomes, indwell time and first stick success of PIVC using B. Braun Peripheral Advantage (PA) by Registered Nurses (RNs). The study will be conducted in the Emergency Department (ED) and/or Medical Surgical (MS) floor(s)/unit(s) in multiple hospitals.

Conditions

• Complications Associated With Device

Interventions

Type	Name	Description
DEVICE	B. Braun Peripheral Advantage (PA) Program	B. Braun PA includes: Christie VeinViewer® Vision2 , Introcan Safety® IV Catheters, STEADYCare™ Smallbore Extension Set, and the PA Education
DEVICE	Hospital Standard of Care	Standard of Care for PIVC access per hospital protocol

Timeline

• Start date: 2020-01-24
• Primary completion: 2021-07-27
• Completion: 2021-07-27
• First posted: 2019-08-07
• Last updated: 2022-08-01
• Results posted: 2022-07-29

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study