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IV SafeLock Device Functionality in Emergency Department

Not Applicable
Completed
Conditions
Intravenous Access
Interventions
Device: IV SafeLock
Registration Number
NCT05695183
Lead Sponsor
Mayo Clinic
Brief Summary

The purpose of this research study is to evaluate the functionality of the IV SafeLock in the clinical emergency department setting.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Emergency Department nurses who are consenting and willing to perform tasks.
  • Their patient population will include stable patients 18 or over, who present through triage, are medically stable, are able to verbally consent and require intravenous access.
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Exclusion Criteria
  • Emergency Department nurses who are unwilling to consent to use IV SafeLock on their patient population.
  • The patient population will exclude pregnant patients, children, prisoners, patients with dementia, or any member of protected class as specified by IRB.
  • The patients must be medically stable and not include patients presenting with acute stroke, acute myocardial infarction, severe sepsis or shock.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Emergency Department NursesIV SafeLockRegistered nurses will use the IV SafeLock Device on patients during care in the emergency department.
Primary Outcome Measures
NameTimeMethod
Functionality of the IV SafeLockBaseline

Measured on a likert scale for nurse evaluation of IV SafeLock

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic Florida

🇺🇸

Jacksonville, Florida, United States

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