Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study

NACompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

July 7, 2015

Primary Completion Date

July 5, 2016

Study Completion Date

December 3, 2018

Conditions
Coronary Artery Disease
Interventions
DEVICE

Resolute Onyx Stent - 2.25 mm - 4.0 mm

Trial Locations (12)

11576

Saint Francis Hospital, Roslyn

19096

Lankenau Medical Center, Wynnewood

27705

Duke University Medical Center, Durham

29621

AnMed Health Medical Center, Anderson

33756

Morton Plant Hospital, Clearwater

37205

Centennial Medical Center, Nashville

44035

University Hospitals Elyria Medical Center, Elyria

46290

St. Vincent Heart Center of Indiana, Indianapolis

58122

Sanford Medical Center, Fargo

62701

Saint John's Hospital, Springfield

75216

Dallas VA Medical Center, Dallas

92037

Scripps Green Hospital, La Jolla

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Medtronic Vascular

INDUSTRY

NCT02419521 - Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Biotech Hunter | Biotech Hunter