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NCT05695183 Clinical Trial

IV SafeLock Device Functionality in Emergency Department

Intravenous Access Clinical Trial

Official title:
Functionality of the IV SafeLock Device in Emergency Department Setting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05695183
Other study ID # 22-012282
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 22, 2023
Est. completion date October 6, 2023

Study information
Verified date October 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date October 6, 2023
Est. primary completion date October 6, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Device:
• IV SafeLock
Designed to prevent patient access to intravenous lines in the hospital setting. The device locks with an institution specific key and protects the hub as well as all tubing access points.

Locations
Country Name City State
United States Mayo Clinic Florida Jacksonville Florida

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Functionality of the IV SafeLock Measured on a likert scale for nurse evaluation of IV SafeLock Baseline
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