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Xarelto Evidence in Real Life of Patients' Preference and Satisfaction Study (X-PRESS)

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Bayer

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Drug: Rivaroxaban (Xarelto, BAY 59-7939)

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

The main objective of the study is to assess preferences of Non Valvular Atrial Fibrillation (NVAF) patients towards different options of an anticoagulation treatment.

Patient preferences for anticoagulant treatment attributes (convenience attributes only), based on a Discrete Choice Experiment(DCE) interview will be elicited and the impact of switching from Vitamin K Antagonist(VKA) to Xarelto® on Atrial Fibrilation(AF) patient treatment satisfaction will be documented, measured by score differences of the Anti-Clot Treatment Scale (ACTS) score in patients switching from VKA to Rivaroxaban.

Enrollment

253 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female and male patients ≥ 20 years of age (legal age limit in Taiwan) with a confirmed diagnosis of AF (non-valvular).
  • Treatment with VKA for at least 6 weeks.
  • Decision to initiate treatment with Rivaroxaban has been made as per investigator's routine treatment practice.
  • Written informed consent of the patient.
  • Wilingness and capability to conduct two F2F interviews.

Exclusion criteria

  • Contraindications to the use of Rivaroxaban as outlined in the local product information .
  • Concomitant treatment with any other anticoagulants.
  • Participation in another study (clinical intervention/observational) within the 3 months prior to enrollment.
  • Patients participating in an investigational program with interventions outside of routine clinical practice.

Trial design

253 participants in 1 patient group

Rivaroxaban, BAY59-7939
Description:
It is a single-arm study in which only patients who switched from a VKA to a NOAC treatment will be included.
Treatment:
Drug: Rivaroxaban (Xarelto, BAY 59-7939)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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