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NCT05695183

IV SafeLock Device Functionality in Emergency Department

Completed NA Last updated 10 October 2023
What this trial tests

NA trial testing IV SafeLock in Intravenous Access in 20 participants. Completed in 6 October 2023.

Timeline
22 July 2023
Primary endpoint
6 October 2023
6 October 2023

Quick facts

Lead sponsorMayo Clinic
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment20
Start date22 July 2023
Primary completion6 October 2023
Estimated completion6 October 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Mayo Clinic

Who can join

18 and older, any sex, with Intravenous Access. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Evaluation of the Functionality in an Emergency Department Setting of an Intravenous Protection Device to Prevent Self-Injection.
    Bragg K, Albus M, Bragg B, Beste RM, et al · · 2024 · cited 3× · PMID 38529519 · DOI 10.2147/mder.s451439

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Other Mayo Clinic trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05695183.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing