Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Acute Coronary Syndromes
  • Atrial Fibrillations
  • Bleeding
  • Coronary Artery Diseases
  • Heart Valve Prostheses
  • Myocardial Infarction
  • Stroke
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The WOEST 2 Registry is a prospective, international, multi-centre, non-interventional, cohort study designed to recruit an unselected cohort of patients with atrial fibrillation and/or a heart valve prosthesis undergoing coronary revascularisation. Trial overview Name : WOEST 2 REGISTRY Target for ...

The WOEST 2 Registry is a prospective, international, multi-centre, non-interventional, cohort study designed to recruit an unselected cohort of patients with atrial fibrillation and/or a heart valve prosthesis undergoing coronary revascularisation. Trial overview Name : WOEST 2 REGISTRY Target for enrollment : 2200 patients Time frame for inclusion : within 72 hours after index PCI or coronary artery bypass grafting (CABG) Follow-up : 24 months Visits : 30 days, 12 and 24 months after index PCI or CABG

Tracking Information

NCT #
NCT02635230
Collaborators
St. Antonius Hospital
Investigators
Principal Investigator: Jurriën M ten Berg, MD, PhD St. Antonius Hospital Nieuwegein, the Netherlands Principal Investigator: Willem JM Dewilde, MD, PhD Imelda Hospital Bonheiden, Belgium