Vascular Closure With Novel External Compression Device: The LockeT Study

Status unconfirmed

Conditions studied: Atrial Fibrillation, Hemostasis

In brief

Single center, retrospective review study comparing Figure of Eight suture to LockeT, enrolling approximately 70 patients.

Key facts

Study ID

NCT06199414

Run by

Kansas City Heart Rhythm Research Foundation

People needed

70

Starts

2024-01-01

Expected to finish

2024-12-01

Last updated by the study team

2024-01-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All participants must meet the following criteria to be included in this study.
• Subjects must be at least 18 years of age.
• Subjects underwent Atrial Fibrillation radiofrequency ablation procedure.
• Subjects must have undergone F-8 or LockeT for venous closure.

You may not qualify if…

• If a subject meet any of the following criteria will be excluded from study participation.
• Subjects under the age of 18.
• Subject's electrophysiology procedure is not planned to access the left atrium or ventricle.
• Subjects in which F-8 or a LockeT was not used.
• If the EP physician detected a formed hematoma prior to venous closure, that patient will be excluded from the study.

Where it is running

• Kansas City Heart Rhythm Institute - Roe Clinic — Overland Park, Kansas, United States
• Overland Park Regional Medical Center — Overland Park, Kansas, United States

Full record on ClinicalTrials.gov

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