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RECRUITING NA

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

NCT06107361 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • DEVICE B. Braun 6.35cm 20 gauge ultralong intravenous catheter
  • DEVICE BD 5.71 cm 20 gauge Accucath

Study Locations (1)

Michigan

  • Beaumont Hospital - Royal Oak — Royal Oak

Trial Details

FieldValue
Enrollment Target 360 participants
Start Date 2023-11-07
Est. Completion 2026-05
Phase NA

Sponsor

Corewell Health East

30 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06107361

The ClinicalTrials.gov registry entry for NCT06107361 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 360 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Corewell Health East, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Peripheral Intravenous Vein Catheter Phlebitis appearing as the primary indexed condition, and to 2 interventions — of which B. Braun 6.35cm 20 gauge ultralong intravenous catheter is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06107361 reports 1 study location spanning 1 distinct geographic area — top geographies include Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06107361 about?

NCT06107361 is a clinical study titled "Evaluating the Role of the Guidewire in Peripheral Intravenous Access: A Randomized Controlled Trial of Ultrasound-Guided Catheter Survival". 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 ...

What is the current status of trial NCT06107361?

This trial is currently recruiting. It is a NA study. The enrollment target is 360 participants. The study started on 2023-11-07. Estimated completion is 2026-05.

What conditions does trial NCT06107361 study?

This clinical trial studies the following conditions: Peripheral Intravenous Vein Catheter Phlebitis, Intravenous Infection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06107361?

The interventions under investigation include: B. Braun 6.35cm 20 gauge ultralong intravenous catheter (DEVICE), BD 5.71 cm 20 gauge Accucath (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06107361?

This trial is sponsored by Corewell Health East, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06107361 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial