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A Study of Participants With Non-Valvular Atrial Fibrillation (NVAF) Treated or Untreated With Oral Anticoagulant in the National Cerebral and Cardiovascular Center (NCVC) in Japan

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status

Completed

Conditions

Non-Valvular Atrial Fibrillation (NVAF)

Study type

Observational

Funder types

Industry

Identifiers

NCT05027061
CV185-771

Details and patient eligibility

About

The purpose of this observational study is to understand real-world oral anticoagulants (OAC) (warfarin, apixaban, dabigatran, edoxaban and rivaroxaban) usage for non-valvular atrial fibrillation (NVAF) patients.

Enrollment

11,776 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Participants received medical treatment for NVAF between 10-Jan-2012 and 31-Aug-2020.

Exclusion criteria

  • Had no data of serum creatinine in the participant's medical records
  • Had no data of body weight in the participant's medical records
  • Were given oral anticoagulant (OAC) for treatment of diseases other than atrial fibrillation (AF)

Other protocol-defined inclusion/exclusion criteria apply.

Trial design

11,776 participants in 6 patient groups

Cohort 1
Description:
Non-valvular atrial fibrillation (NVAF) participants receiving oral anticoagulant - Warfarin
Cohort 2
Description:
NVAF participants receiving oral anticoagulant - Apixaban
Cohort 3
Description:
NVAF participants receiving oral anticoagulant - Dabigatran
Cohort 4
Description:
NVAF participants receiving oral anticoagulant - Edoxaban
Cohort 5
Description:
NVAF participants receiving oral anticoagulant - Rivaroxaban
Cohort 6
Description:
NVAF participants not receiving oral anticoagulants

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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