Clinical Trials Directory

Trials / Completed

CompletedNCT02559232

An Observational Cross-sectional Study Evaluating the Use of Re-sources and the Sociodemographic and Clinical Characteristics of Patients Diagnosed With Non-valvular Atrial Fibrillation With a Risk of Stroke or Systemic Embolism on Anticoagulant Therapy and Treated in Primary Care Centers

An Observational Cross-sectional Study Evaluating the Use of Re-sources and the Sociodemographic and Clinical Characteristics of Patients Diagnosed With NVAF With a Risk of Stroke or Systemic Embolism on Anticoagulant Therapy and Treated in Primary Care Centers

Status
Completed
Phase
Study type
Observational
Enrollment
247 (actual)
Sponsor
Bayer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a retrospective observational study to describe the sociodemographic and clinical characteristics of patients diagnosed with non-valvular atrial fibrillation (NVAF) at risk of stroke or systemic embolism, who at least three months ago changed their anticoagulant therapy, due to any clinical situation, and are currently on treatment with a direct oral anticoagulant (DOAC)

Conditions

Interventions

TypeNameDescription
DRUGDirect Oral Anticoagulant (DOAC)Treatment pattern following the summary of product characteristics

Timeline

Start date
2015-09-01
Primary completion
2015-12-01
Completion
2016-03-01
First posted
2015-09-24
Last updated
2017-02-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT02559232. Inclusion in this directory is not an endorsement.