Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

Japanese Anti-Coagulation Regimen Exploration in AF Catheter Ablation Registry - Rivaroxaban cohort

Trial Profile

Japanese Anti-Coagulation Regimen Exploration in AF Catheter Ablation Registry - Rivaroxaban cohort

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 10 Oct 2017

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Rivaroxaban (Primary)
  • Indications Thromboembolism
  • Focus Adverse reactions; Therapeutic Use
  • Acronyms JACRE-R
  • Sponsors Bayer Yakuhin

Most Recent Events

  • 28 Sep 2017 Results assessing the effects and risks of heparin bridging and different patterns of interruption/resumption of rivaroxaban on complications of catheter ablation for atrial fibrillation ,published in the Circulation Journal
  • 30 Aug 2017 Results a sub-analysis of JACRE Registry (n=1322; JACRE-R and JACRE-W )presented at the ESC Congress 2017: Annual Congress of the European Society of Cardiology
  • 25 Oct 2016 Results assessing safety and efficacy from Rivaroxaban cohort (JACRE-R) and Warfarin cohort (JACRE-W) studies published in the Circulation Journal.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top