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NCT02654470

Watchman FLX Left Atrial Appendage Closure Device Post Approval Study ( Europe Only)

Completed Last updated 19 November 2021
What this trial tests

trial testing Watchman FLX in Non-valvular Atrial Fibrillation in 300 participants. Completed in 28 September 2021.

Timeline
16 July 2019
Primary endpoint
28 September 2021
28 September 2021

Quick facts

Lead sponsorBoston Scientific Corporation
StatusCompleted
Study typeOBSERVATIONAL
Enrollment300
Start date16 July 2019
Primary completion28 September 2021
Estimated completion28 September 2021
Sites17 locations across Denmark, France, Italy, Netherlands, Ireland, United Kingdom, Germany, Poland

Drugs / interventions tested

Conditions studied

Sponsor

Boston Scientific Corporation — full company profile →

Who can join

18 and older, any sex, with Non-valvular Atrial Fibrillation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Watchman FLX Left Atrial Appendage Closure Device Post Approval Study

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Real-world clinical outcomes with a next-generation left atrial appendage closure device: the FLXibility Post-Approval Study.
    Betts TR, Grygier M, Nielsen Kudsk JE, Schmitz T, et al · · 2023 · cited 25× · PMID 36734247 · DOI 10.1093/europace/euac270

Verify or expand the search:

Other recruiting trials for Non-valvular Atrial Fibrillation

Currently open trials in the same condition.

Other Boston Scientific Corporation trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02654470.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing