Clinical Trial Details

Overview

Research Study Summary

Outcomes Registry for Better Informed Treatment of Atrial Fibrillation II - ORBIT AF II - Phase II of the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF II) is designed to evaluate the utilization of target-specific antithrombotic agents, such as factor Xa (FXa) inhibitors and direct thrombin inhibitors, and associated outcomes.

Purpose

The goal of this US prospective outpatient AF registry is to identify real world treatment patterns in patients with AF(atrial fibrillation), outside of randomized controlled trials. Specifically, the registry will attempt to define current treatment patterns and their relationship with outcomes, including stroke, all-cause mortality, and quality-of-life.

To Learn more

CW ID: 192703
Date Last Changed: January 17, 2014

Clinical Trial Snapshot

Phase
2
Gender
Both Male and Female
Age
21 and up
Overall Status
Recruiting
Facility Type

Eligibility

Inclusion:

  • Be an adult, 21 years of age or older.
  • Have electrocardiographically confirmed AF.
  • New-onset/first-detected AF diagnosed within the 6 months preceding the baseline visit OR
  • Initiated or transitioned to a FXa inhibitor or a direct thrombin inhibitor within the 3 months preceding the baseline visit.
  • AND OTHERS

Exclusion:

  • Have atrial flutter only.
  • Have an anticipated life expectancy less than 6 months.
  • . Have transient AF secondary to a reversible condition (eg, hyperthyroidism, pulmonary embolism, post-cardiothoracic surgery).
  • Is participating in a randomized clinical study of any anticoagulation for AF at the time of enrollment.
  • Was enrolled in the ORBIT-AF I registry.
  • AND OTHERS

Contact

Wendy Schneider, MSN, Clinical Research Coordinator
Holy Cross Jim Moran Heart and Vascular Research Institute
2901 Coral Hills Drive, Suite 240
Coral Springs, FL 33065
Phone: (954) 346-0864
Fax: (954) 753-8067

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