IV SafeLock Device Functionality in Emergency Department

Mayo Clinic

Status: Completed

Conditions: Intravenous Access

Treatments: Device: IV SafeLock

Study type: Interventional

Funder types: Other

Identifiers

NCT05695183

22-012282

Details and patient eligibility

About

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

Enrollment: 20 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Emergency Department Nurses

Experimental group

Description:

Registered nurses will use the IV SafeLock Device on patients during care in the emergency department.

Treatment:

Device: IV SafeLock