IV SafeLock Device Functionality in Emergency Department
Not Applicable
Completed
- Conditions
- Intravenous Access
- 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.
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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Functionality of the IV SafeLock Baseline Measured on a likert scale for nurse evaluation of IV SafeLock
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic Florida
🇺🇸Jacksonville, Florida, United States
Mayo Clinic Florida🇺🇸Jacksonville, Florida, United States