RIVS (AccuCath Device) Versus (Conventional) PIV Catheter

Status Recruiting

Clinical Trial Summary

The study will test a hypothesis that the AccuCath™ System will have a higher rate of successful first attempt peripheral IV placement, higher completion of therapy, fewer complications, longer dwell times and higher user satisfaction compared to Conventional IV Catheters.

Clinical Trial Description

This study is designed to evaluate user/physician preference as it relates to use of a 510(k) cleared vascular access and catheter device compared with conventional needle/catheter vascular access devices, in terms of first stick success rates, dwell time, device related vascular complications and adverse events and overall user and patient satisfaction. As noted above, the study is designed to formally test the hypothesis that the AccuCath™ System will exhibit superiority in terms of the rate of successful first attempt peripheral IV placement, higher completion of therapy, fewer complications, longer dwell times and higher user satisfaction compared to Conventional IV Catheters. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Vascular Access Complication

Clinical Trial Details

NCT number	NCT01943474
Study type	Interventional
Source	Vascular Pathways, Inc.
Contact	Bette Idemoto, PhD, RN
Phone	216-844-2202
Email	bette.idemoto@uhhospitals.org
Status	Recruiting
Phase	N/A
Start date	April 2013
Completion date	October 2013

View Details

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