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Discontinuation for Oral Anticoagulants in Patients With Atrial Fibrillation

H

Hospital Italiano de Buenos Aires

Status

Unknown

Conditions

Auricular Fibrillation
Anticoagulant Drugs

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04133545
Protocol_3525

Details and patient eligibility

About

The purpose of this study is to compare the discontinuation rates for vitamin K antagonists and for direct oral anticoagulants during their first year

Full description

The purpose of this study is to compare the discontinuation rates for vitamin K antagonists and for direct oral anticoagulants during their first year of use after their initiation during hospitalization in patients covered by our health insurance plan.

Enrollment

360 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient older than 18 years of age covered by our Health Care Insurance Plan.
  2. Indication for oral anticoagulation with an expected duration of use of no less than 1 year.

Exclusion criteria

  1. Refusal to take part.
  2. Use of oral anticoagulants within 6 months prior to admission.
  3. Presence of mechanical prosthetic valve.
  4. Chronic renal failure with creatinine clearance <30 mL/min (estimated using the MDRD formula).

Trial design

360 participants in 2 patient groups

DOAC
Description:
Direct oral anticoagulant
OAC
Description:
Vitamin K anticoagulant

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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