Completed NA INTERVENTIONAL 1-arm NCT01937195

AccuCath™ Intravenous (IV) Device Used by Vascular Access Team (VAT)

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

Sponsor: C. R. Bard

Conditions Vascular Access Complication

Interventions AccuCath Intravenous Catheter System

Updated 9 times since 2017 Last updated: Mar 9, 2017 Started: Apr 30, 2013 Primary completion: Jul 31, 2014 Completion: Nov 30, 2014

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT01937195, this NA trial focuses on Vascular Access Complication and remains completed. Sponsored by C. R. Bard, it has been updated 9 times since 2013, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

Change History

9 versions recorded

Sep 2024 — Present [monthly]

Completed NA
Jul 2024 — Sep 2024 [monthly]

Completed NA
Jan 2023 — Jul 2024 [monthly]

Completed NA
Dec 2022 — Jan 2023 [monthly]

Completed NA
Jan 2021 — Dec 2022 [monthly]

Completed NA

▶ Show 4 earlier versions

Jun 2018 — Jan 2021 [monthly]

Completed NA
Jun 2017 — Jun 2018 [monthly]

Completed NA

Status: Unknown Status → Completed
Feb 2017 — Jun 2017 [monthly]

Unknown Status NA
Jan 2017 — Feb 2017 [monthly]

Unknown Status NA

First recorded

Apr 2013

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

C. R. Bard

Data source: C. R. Bard

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Lewisburg, United States