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Anticoagulant Utilization Pattern

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Atrial Fibrillation

Study type

Observational

Funder types

Industry

Identifiers

NCT01847560
1160.177

Details and patient eligibility

About

This study plans to describe utilization patterns for oral anticoagulants over time in patients with non-valvular atrial fibrillation at risk for stroke using electronic claims data from a United States commercial insurance database.

Enrollment

333,664 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A recorded diagnosis of atrial fibrillation
  • Initiation of oral anticoagulant medication
  • Congestive Heart Failure, Hypertension, Age > 75, Diabetes Mellitus, Prior Stroke or Transient Ischemic Attack, Vascular Disease, Age 65-74, Sex Category (CHA2DS2-VASc) Score >=1
  • At least 18 years of age on the date of anticoagulant initiation

Exclusion criteria

  • Patients with missing or ambiguous age or sex information
  • Patients with documented evidence of valvular disease
  • Patients with less than 12 months enrolment in the UnitedHealth Research Database preceding the first dispensing
  • Patients with prior use of any oral anticoagulant

Trial design

333,664 participants in 2 patient groups

Dabigatran
Warfarin or other New Oral Anticoagulant (NOAC)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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