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IV SafeLock Device Functionality in Emergency Department

NCT05695183 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2023-10-10

No results posted yet for this study

Summary

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

Conditions

  • Intravenous Access

Interventions

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.

Sponsors & Collaborators

Principal Investigators

  • Kara Bragg, APRN, DNP · Mayo Clinic

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-07-22
Primary Completion
2023-10-06
Completion
2023-10-06

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05695183 on ClinicalTrials.gov