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NCT04590898

Peri-device Leakage Closure After LAAO

Completed Last updated 22 July 2022
What this trial tests

trial testing Peri-device leakage closure after left atrial appendage occlusion in Atrial Fibrillation in 85 participants. Completed in 1 September 2021.

Timeline
27 September 2020
Primary endpoint
1 September 2021
1 September 2021

Quick facts

Lead sponsorCardiovascular Center Frankfurt
StatusCompleted
Study typeOBSERVATIONAL
Enrollment85
Start date27 September 2020
Primary completion1 September 2021
Estimated completion1 September 2021
Sites16 locations across Denmark, United Kingdom, Germany, Poland, Switzerland, United States, Spain

Drugs / interventions tested

Conditions studied

Sponsor

Cardiovascular Center Frankfurt

Who can join

Adults 18 to 100, any sex, with Atrial Fibrillation or Stroke. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators thought to evaluate the safety and feasibility of peri-device leakage closure after left atrial appendage occlusion (LAAO, either surgical or interventional) with different devices.

Publications & conference data

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

  1. Safety and feasibility of peri-device leakage closure after LAAO: an international, multicentre collaborative study.
    Piayda K, Sievert K, Della Rocca DG, Adeola OG, et al · · 2021 · cited 20× · PMID 34219662 · DOI 10.4244/eij-d-21-00286

Verify or expand the search:

Other recruiting trials for Atrial Fibrillation

Currently open trials in the same condition.

Other Cardiovascular Center Frankfurt trials

Trials by the same sponsor.

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Data sources for this page

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