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Mobile App for Improving Adherence of Rivoxaban (RIVOX-AF)

Seoul National University logo

Seoul National University

Status

Enrolling

Conditions

Atrial Fibrillation

Treatments

Device: MEDI-app

Study type

Interventional

Funder types

Other

Identifiers

NCT05557123
RIVOX-AF

Details and patient eligibility

About

RIVOX-AF study is a prospective, multicenter, randomized controlled study in which patients with AF are allocated to medication-app group or conventional treatment group. The App based feed-back algorithm will provide the patients with check taking drug or reminding of taking drug.

Enrollment

1,042 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with AF aged 19 years or older with one or more comorbidities including heart failure, myocardial infarction, stable angina, hypertension or diabetes mellitus (Patients can be enrolled 3 months after myocardial infarction or percutaneous coronary intervention).
  • patients who already took or plan to take rivoxban
  • patients who able to use smart phone

Exclusion criteria

  • creatinine clearance <15ml/min
  • moderate or severe mitral stenosis
  • mitral valve operation history
  • current alcohol abuse or alcohol abus history
  • Not eligible for study due to legal or psychiatric problem
  • enrolled other clinical study within 4 weeks
  • declined to enroll the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,042 participants in 2 patient groups

MEDI-app
Experimental group
Description:
conventional treatment with MEDI-app feedback
Treatment:
Device: MEDI-app
conventional treatment
No Intervention group
Description:
conventional treatment

Trial contacts and locations

1

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Central trial contact

Minjae Yoon, MD; Dong-Ju Choi, MD, PhD

Data sourced from clinicaltrials.gov

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