At a glance
ClinicalIndex Comparison RecordN/ACompleted· 434 enrolled
Drug / intervention
Not specified
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 for Cardiac Ablation Registry (VACCAR)
In Brief
An observational study for Atrial Fibrillation. Completed, enrolled 434 participants across 1 site.
Detailed Summary
The objective of this registry is to find out if there is a difference in patient satisfaction and rate of vascular and bleeding complications with use of Perclose Proglide system or F08S for venous closure post atrial fibrillation and atrial flutter procedures in comparison to manual compression.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsAtrial Fibrillation
CountriesUnited States
CollaboratorsAbbott Medical Devices
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartOct 2017
First PostedJun 2018
Primary CompletionMay 2019
TodayJul 2026
First PostedJun 6, 2018
Enrollment StartOct 25, 2017
Primary CompletionMay 24, 2019
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 8.1 years ago