RecruitingACTRN12624001147572

Introducing a Vascular Access Specialist Model in the Emergency Department (VAS-ED)

Effect of Introducing a Vascular Access Specialist Model on First Insertion Success Rates for Adult Patients in the Emergency Department (VAS-ED)


Sponsor

Royal Brisbane and Women's Hospital

Enrollment

320 participants

Start Date

Feb 4, 2025

Study Type

Interventional

Conditions

Summary

The primary aim of this randomised controlled trial (RCT) is to compare the clinical and cost eff ectiveness of new Vascular Access Specialist model with the Generalist inserter model (inserted by a doctor or nurse in emergency department). You may be eligible to participate in this trial if you are an emergency department patient more than theage of 18 and are requiring a peripheral venous catheter inserted as part of your therapy. All participants enrolled in this trial will be randomly allocated (by chance) to receive one of two options (inserted by either a Vascular Access Specialist or a doctor/nurse in emergency department). Participants and families will be asked to rate the satisfaction of the insertion, and the peripheral intravenous catheter will be observed closely to examine side effects. It is hoped that the findings of this trial will provide information on which insertion model is the most effective in preventing first insertion failure.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

Almost every patient admitted to hospital through the emergency department needs an intravenous (IV) line — a small tube inserted into a vein to deliver fluids or medications. First-attempt success rates for inserting these lines vary widely, and failed attempts can be painful and delay treatment. This study is testing whether having a specialist Vascular Access Nurse insert the IV line leads to better outcomes compared to the usual approach where any available doctor or nurse does it. Participants will be randomly assigned to have their IV line inserted by either a Vascular Access Specialist or the usual emergency department clinician. Both groups will be watched closely for complications like failed insertions, infection, or blockage, and patients will be asked about their comfort and satisfaction. You may be eligible if you are 18 or older, have come through the emergency department, are likely to be admitted to hospital, and need IV therapy for at least 24 hours. People needing urgent resuscitation (triage category 1), those receiving end-of-life care, and non-English speakers without an interpreter are not eligible. This study could lead to safer, less uncomfortable IV line insertions across Australian hospitals.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Participants in this study are patients who require intravenous catheters (IVC) in emergency departments (ED). Consenting participants will receive a IVC inserted by a Vascular Access Specialist (nurs

Participants in this study are patients who require intravenous catheters (IVC) in emergency departments (ED). Consenting participants will receive a IVC inserted by a Vascular Access Specialist (nurses trained in ultrasound-guided IVC insertion) in the intervention group when a PIVC is required in ED. The IVC will remain in situ as long as it is required as per hospital policy. The insertion length of the IVC vary depending on the complexity of patient's venous condition and device is required. Patients will be monitored daily by a research nurse.


Locations(1)

Royal Brisbane & Womens Hospital - Herston

QLD, Australia

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ACTRN12624001147572