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Catheter Precision, Inc. (NYSE:VTAK), a US based innovative medical device company, announced today the publication of its first LockeT study in the Journal of Cardiovascular Electrophysiology. The study titled, Feasibility, safety and efficacy of a novel external compression vascular closure device: The LockeT Study, was made available online on August 5, 2024.
The study demonstrates the first clinical use of LockeT in 102 patients utilizing 182 LockeT devices and suggests that LockeT is effective for hemostasis, and early ambulation can be achieved with no major complications. The use of LockeT appears to generate the same benefits as standard of care (manual compression) without needing prolonged bed rest or monitoring, facilitating early mobilization and same-day discharge. Highlights of the study include:
Hemostasis was immediately achieved
Hemostasis remained at 2 hours in 98% of patients
No major complications were observed
The majority of patients were discharged same day
Average Time to ambulation was under 4 hours
Further studies with LockeT are underway and the next study is planned to be concluded this year with additional data.
Posted In: VTAK
