Status:
COMPLETED
Edoxaban in Patients With Non-valvular Atrial Fibrillation Undergoing Percutaneous Coronary Intervention
Lead Sponsor:
Daiichi Sankyo
Collaborating Sponsors:
Daiichi Sankyo Deutschland GmbH
Conditions:
Non-valvular Atrial Fibrillation
Eligibility:
All Genders
18+ years
Brief Summary
This study is designed to gain real-world clinical data on the peri- and post-procedural usage of anticoagulation and antiplatelet therapy in patients with non-valvular atrial fibrillation (NVAF) unde...
Detailed Description
The study will assess real-world evidence data of anticoagulation and antiplatelet therapy in patients with NVAF undergoing PCI treated with edoxaban. The observation period will start 4 to 72 hours a...
Eligibility Criteria
Inclusion
- ≥ 18 years of age
- Providing written informed consent (ICF) for participation in the study
- NVAF treated with edoxaban
- Successful PCI
- No planned elective cardiac intervention for the whole duration of the study (up to 1 year)
- Capability of patients for follow-up by telephone by the site for the whole duration of the study (up to 1 year)
- Availability of patients for follow-up by telephone by the site for the whole duration of the study (up to 1 year)
- Willingness of patients for follow-up by telephone by the site for the whole duration of the study (up to 1 year)
- Not simultaneously participating in any interventional study
- Life expectancy \> 1 year
Exclusion
- Not applicable
Key Trial Info
Start Date :
June 30 2020
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
July 6 2023
Estimated Enrollment :
666 Patients enrolled
Trial Details
Trial ID
NCT04519944
Start Date
June 30 2020
End Date
July 6 2023
Last Update
August 2 2023
Active Locations (66)
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1
Zentralklinik Bad Berka
Bad Berka, Germany, 99437
2
SLK-Kliniken Heilbronn GmbH Klinikum am Plattenwald
Bad Friedrichshall, Germany, 74177
3
Kerckhoff-Klinik GmbH
Bad Nauheim, Germany, 61231
4
Herz- und Diabeteszentrum Nordrhein-Westfalen
Bad Oeynhausen, Germany, 32545