Ignite Creation Date:
2024-05-06 @ 1:57 AM
Last Modification Date:
2024-10-26 @ 11:12 AM
Study NCT ID:
NCT01937195
Status:
COMPLETED
Last Update Posted:
2017-04-20
First Post:
2013-04-15
Brief Title:
AccuCath Intravenous IV Device Used by Vascular Access Team VAT
Sponsor:
C R Bard
Organization:
C R Bard
Study Overview
Official Title:
A Prospective Randomized Controlled Multicenter Comparison Between the AccuCath Intravenous Catheter System With Retractable Coiled Tip Guidewire and Conventional Peripheral Intravenous Catheters With a Vascular Access Team
Status:
COMPLETED
Status Verified Date:
2017-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The study will test a hypothesis that the AccuCath System will have a higher rate of successful first attempt peripheral intravenous PIV placement higher completion of therapy fewer complications longer dwell times and higher user satisfaction compared to Conventional IV Catheters
Detailed Description:
Phase One is designed as a one-arm prospective study to compare patients using the AccuCath Intravenous Catheter System to the results found in literature Phase Two is designed as a two-arm prospective randomized controlled study comparing the AccuCath Intravenous Catheter System to conventional PIV catheters This study site will be completing Phase One only
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None