Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Chronic Total Occlusion of Coronary Artery
  • Coronary (Artery) Disease
  • Percutaneous Coronary Intervention
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

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

Description

This is prospective, dual-arm, randomized, multi-center, observational study comparing patient outcomes and staff radiation exposure in chronic total occlusion PCI procedures through 48 hours post procedure or hospital discharge, whichever occurs first.

This is prospective, dual-arm, randomized, multi-center, observational study comparing patient outcomes and staff radiation exposure in chronic total occlusion PCI procedures through 48 hours post procedure or hospital discharge, whichever occurs first.

Tracking Information

NCT #
NCT03959072
Collaborators
Not Provided
Investigators
Principal Investigator: William Lombardi (Acting), MD University of Washington Principal Investigator: William Nicholson (Emeritus), MD WellSpan York Hospital