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RECRUITING
NCT06107361
NA

Evaluating the Role of the Guidewire in Peripheral Intravenous Access: A Randomized Controlled Trial of Ultrasound-Guided Catheter Survival

Sponsor: Corewell Health East

View on ClinicalTrials.gov

Summary

This is a prospective, parallel, non-blinded, two-arm randomized controlled trial of intravenous catheter failure evaluating the impact of a built-in guide wire. The objective of this study is to demonstrate that the control ultralong intravenous catheter (IV) without the guide wire is non-inferior to the experimental catheter with the guide wire. After obtaining consent, eligible patients will be randomly allocated to control Arm 1 (ultralong intravenous catheter) or experimental Arm 2 (ultralong intravenous catheter with guide wire) in a ratio of 1:1 via a computer-generated randomization schedule. The participants will be followed to collect data until the catheter is removed.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

360

Start Date

2023-11-07

Completion Date

2026-05

Last Updated

2026-01-16

Healthy Volunteers

No

Interventions

DEVICE

B. Braun 6.35cm 20 gauge ultralong intravenous catheter

B Braun Medical Inc, 6.35cm 20 gauge ultralong intravenous catheter

DEVICE

BD 5.71 cm 20 gauge Accucath

Bard Access Systems, Inc, BD 5.71 cm 20 gauge ultralong intravenous catheter with guide wire

Locations (1)

Beaumont Hospital - Royal Oak

Royal Oak, Michigan, United States