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Clinical trialNCT05101993CompletedInterventional

VCLIP Post-Market Study, Long-term Follow-up on LAA Exclusion Using AtriClip

SponsorAtriCure, Inc.Enrollment156Left Atrial Appendage Absent
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Retrospective-prospective, multi-center, non-randomized, unblinded, post-market study to evaluate the long-term performance and safety of AtriClip® FLEX-V LAA and PRO•V LAA Exclusion devices for exclusion of the left atrial appendage of the heart during concomitant cardiac procedures.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Franciscan Health

    Indianapolis, Indiana, United States

  • Washington University School of Medicine

    St Louis, Missouri, United States

  • Albany Medical College

    Albany, New York, United States

  • Columbia University

    New York, New York, United States

  • Mount Sinai

    New York, New York, United States

  • Nyu

    New York, New York, United States

  • Mercy Health Cincinnati

    Cincinnati, Ohio, United States

  • Toledo Hospital

    Toledo, Ohio, United States

  • Prisma Health

    Greenville, South Carolina, United States

  • Centra Lynchburg General Hospital

    Lynchburg, Virginia, United States

  • Aurora Research Institute Llc

    Milwaukee, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
27 Jan 2022
Primary completion
31 Mar 2023
Completion
22 Jul 2024
Last update posted
3 Jul 2025
Registered enrollment
156
Registry id
NCT05101993

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.