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NCT02690155 · ClinicalTrials.gov registry record

Real-world Comparative Effectiveness of Rivaroxaban Versus VKA

A clinical trial of Atrial Fibrillation, sponsored by Bayer.

Completed
Registry status
38,831
Enrollment target
1
Study location

NCT02690155: Completed study of Atrial Fibrillation, sponsored by Bayer.

NCT02690155 is a study of Atrial Fibrillation that has completed, run by Bayer. The registered enrollment target is 38,831 participants, above the 2,805-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (1284% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02690155, a study of Atrial Fibrillation, has completed, sponsored by Bayer.

COMPLETED
Registry status
38,831 participants
Enrollment target
1
Study location

Study Summary

To obtain a better understanding on the comparative effectiveness of rivaroxaban versus VKA(Vitamin K antagonist) for stroke prevention in patients with NVAF(non-valvular atrial fibrillation) in a real-life setting

Conditions Studied

Interventions

  • DRUG Rivaroxaban (Xarelto, BAY59-7939)
  • DRUG VKA (Vitamin K antagonist)

Study Locations (1)

New York

  • - New York

Trial Details

FieldValue
Enrollment Target 38,831 participants
Start Date 2016-02-12
Est. Completion 2016-03-01
Bayer

591 total trials

What the finished NCT02690155 record still lists

NCT02690155 is an observational study that tracks outcomes without assigning an intervention. Its 38,831 participants enrollment target places it among the larger protocols in the corpus, above the 2,805-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (1284% higher).

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 2 interventions - of which Rivaroxaban (Xarelto, BAY59-7939) is the first listed.

NCT02690155 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT02690155 about?

NCT02690155 is a clinical study titled "Real-world Comparative Effectiveness of Rivaroxaban Versus VKA". To obtain a better understanding on the comparative effectiveness of rivaroxaban versus VKA(Vitamin K antagonist) for stroke prevention in patients with NVAF(non-valvular atrial fibrillation) in a real-life setting

What is the current status of trial NCT02690155?

This trial is currently completed. The enrollment target is 38,831 participants. The study started on 2016-02-12. Estimated completion is 2016-03-01.

What conditions does trial NCT02690155 study?

This clinical trial studies the following conditions: Atrial Fibrillation.

What interventions are being tested in trial NCT02690155?

The interventions under investigation include: Rivaroxaban (Xarelto, BAY59-7939) (DRUG), VKA (Vitamin K antagonist) (DRUG).

Who is sponsoring clinical trial NCT02690155?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02690155 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Atrial Fibrillation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02690155's enrollment target sits among peer trials

38,831 3rd of 202 higher than 200 of 202 other Atrial Fibrillation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02690155, the US trial registry maintained by the National Library of Medicine. NCT02690155 (large enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.