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NCT04590898 · ClinicalTrials.gov registry record

Peri-device Leakage Closure After LAAO

A clinical trial of Stroke and Atrial Fibrillation, sponsored by Cardiovascular Center Frankfurt.

Completed
Registry status
85
Enrollment target
16
Study locations

NCT04590898 is a study of Stroke and Atrial Fibrillation that has completed, run by Cardiovascular Center Frankfurt. The registered enrollment target is 85 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (99% lower). The trial reports 16 study locations across 10 states.

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The verdict

NCT04590898, a study of Stroke and Atrial Fibrillation, has completed, sponsored by Cardiovascular Center Frankfurt.

COMPLETED
Registry status
85 participants
Enrollment target
16
Study locations

Study Summary

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.

Interventions

  • DEVICE Peri-device leakage closure after left atrial appendage occlusion

Study Locations (16)

Other

  • Aarhus University Hospital - Aarhus
  • Rigshospitalet Copenhagen - Copenhagen
  • Universitätsmedizin Berlin - Campus Benjamin Franklin (CBF) - Berlin
  • Poznan University of Medical Sciences - Poznan
  • Hospital Universitario de Salamanca - Salamanca
  • Inselspital Bern - Bern
  • Nuffield Health - Headington

Arizona

  • • Banner University Medical Center Phoenix - Phoenix

California

  • Scripps Health - La Jolla

Kansas

  • Kansas City Heart Rhythm Institute - Overland Park

Minnesota

  • Mayo Clinic Hospital - Saint Mary's Campus - Rochester

Tennessee

  • Vanderbilt Heart Institute - Nashville

Texas

  • Austin Heart - Austin

Utah

  • University of Utah Hospital - Salt Lake City

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2020-09-27
Est. Completion 2021-09-01

Sponsor

Cardiovascular Center Frankfurt

1 total trials

What the Registry Record Tells You About NCT04590898

The ClinicalTrials.gov registry entry for NCT04590898 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 85 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (99% lower). The listed sponsor is Cardiovascular Center Frankfurt, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Stroke appearing as the primary indexed condition, and to 1 intervention - of which Peri-device leakage closure after left atrial appendage occlusion is the first listed.

NCT04590898 reports 16 study locations spanning 10 distinct geographic areas - top geographies include Other, Arizona, California.

Frequently Asked Questions

What is clinical trial NCT04590898 about?

NCT04590898 is a clinical study titled "Peri-device Leakage Closure After LAAO". 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.

What is the current status of trial NCT04590898?

This trial is currently completed. The enrollment target is 85 participants. The study started on 2020-09-27. Estimated completion is 2021-09-01.

What conditions does trial NCT04590898 study?

This clinical trial studies the following conditions: Stroke, Atrial Fibrillation, Bleeding, Leakage of Cardiac Device.

What interventions are being tested in trial NCT04590898?

The interventions under investigation include: Peri-device leakage closure after left atrial appendage occlusion (DEVICE).

Who is sponsoring clinical trial NCT04590898?

This trial is sponsored by Cardiovascular Center Frankfurt, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04590898 being conducted?

This trial has 16 study locations across Arizona, California, Kansas, Minnesota, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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