Transforming PCI Informed Consent Into an Evidence-based Decision-making Tool

CompletedOBSERVATIONAL
Enrollment

1,399

Participants

Timeline

Start Date

September 30, 2009

Primary Completion Date

October 31, 2011

Study Completion Date

September 30, 2012

Conditions
Non-emergent Percutaneous Coronary Intervention (PCI)
Trial Locations (7)

48202

Henry Ford Health System, Detroit

62701

Prairie Education and Research Cooperative, Springfield

63130

Barnes-Jewish Hospital/Washington University School of Medicine, St Louis

64111

Saint Luke's Hospital of Kansas City, Kansas City

75204

Baylor Research Institute, Plano

94612

Kaiser Permanente, Oakland

01199

Baystate Medical Center, Springfield

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Washington University School of Medicine

OTHER

collaborator

Baylor Research Institute

OTHER

collaborator

Baystate Medical Center

OTHER

collaborator

Henry Ford Health System

OTHER

collaborator

Kaiser Permanente

OTHER

collaborator

Prairie Education and Research Cooperative

INDUSTRY

lead

Saint Luke's Health System

OTHER

NCT01383382 - Transforming PCI Informed Consent Into an Evidence-based Decision-making Tool | Biotech Hunter | Biotech Hunter