A U.S Post Approval Study Evaluating the SYNERGY XLV (MEGATRON) Stent System

CompletedOBSERVATIONAL
Enrollment

100

Participants

Timeline

Start Date

April 14, 2021

Primary Completion Date

August 19, 2022

Study Completion Date

August 18, 2023

Conditions
AtherosclerosisHeart Diseases, CoronaryCoronary Artery DiseaseCardiovascular Diseases
Interventions
DEVICE

SYNERGY XLV (Megatron) Coronary Stent System

The SYNERGY MEGATRON Everolimus-Eluting Platinum Chromium Coronary Stent System is indicated for improving luminal diameter in patients, including those at high risk for bleeding, with diabetes mellitus, with symptomatic heart disease, stable angina, unstable angina, non-ST elevation MI or documented silent ischemia due to atherosclerotic lesions in native coronary arteries \>3.50 mm to \<5.00 mm in diameter in lesions \<28 mm in length.

Trial Locations (8)

22042

Inova Fairfax Hospital, Fairfax

27607

Wake Medical Center, Raleigh

33756

Clearwater Cardiovascular Consultants, Clearwater

64116

North Kansas City Hospital, Kansas City

75226

Baylor Heart and Vascular Hospital, Dallas

97239

Oregon Health Sciences University, Portland

06520

Yale University, New Haven

02215

Beth Israel Deaconness Medical Center, Boston

Sponsors
All Listed Sponsors
lead

Boston Scientific Corporation

INDUSTRY