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Be Part of Research - Trial Details - Study in Atrial Fibrillation (AF) Patients at High Risk of Stroke

Study in Atrial Fibrillation (AF) Patients at High Risk of Stroke

Not Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Atrial Fibrillation


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The GARDENIA registry will collect real-world clinical data on the anticoagulant strategies in patients with AF at elevated risk of stroke but also elevated risk of bleeding.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Sep 2022 Mar 2025

OBSERVATIONAL



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Anthos Investigate Site
    Peterborough
    Cambridgeshite
    PE3 9GZ
  • Anthos Investigate Site
    Hayle
    Cornwall
    TR27 5DT
  • Anthos Investigate Site
    Norwich
    Norfolk
    NR2 2TJ
  • Anthos Investigate Site
    Corby
    Northamptonshire
    NN17 2UR
  • Anthos Investigate Site
    Ashington
    Northumberland
    NE63 9JJ
  • Anthos Investigate Site
    Newcastle
    Tyne & Wear
    NE7 7DN
  • Anthos Investigative Site
    Barry
    Vale Of Glamorgan
    CF63 1BA
  • Anthos Investigate Site
    Middlesex
    TW7 6AF


The study is sponsored by Anthos Therapeutics, Inc. and is in collaboration with CYTE Global.




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Read full details for Trial ID: NCT05421533
Last updated 02 October 2024

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.