At a glance
ClinicalIndex Comparison RecordN/AUnknown· 70 target
Drug / intervention
Venous Closuredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Vascular Closure With Novel External Compression Device After Atrial Fibrillation Ablation: The LockeT Study
In Brief
An observational study evaluating Venous Closure for Atrial Fibrillation and Hemostasis. Targeting 70 participants across 2 sites.
Detailed Summary
Single center, retrospective review study comparing Figure of Eight suture to LockeT, enrolling approximately 70 patients.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsAtrial Fibrillation, Hemostasis
CountriesUnited States
Collaborators--
Timeline
N/AUnknownOverdue
202420252026
Enrollment StartJan 2024
First PostedJan 2024
Primary CompletionOct 2024
Study CompletionDec 2024
TodayJul 2026
First PostedJan 10, 2024
Enrollment StartJan 1, 2024
Primary CompletionOct 1, 2024
Study CompletionDec 1, 2024
TodayJul 1, 2026
Enrollment to primary: 9 monthsPosted 2.5 years ago
Interventions
Venous Closuredevice
Vascular closure to achieve vascular hemostasis following femoral access with large bore sheaths in catheter ablation procedures