PLATINUM Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions-Pharmacokinetics (PLATINUM PK)

PHASE3CompletedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

October 31, 2009

Primary Completion Date

February 28, 2010

Study Completion Date

May 31, 2015

Conditions
Coronary Artery Disease
Interventions
DEVICE

PROMUS Element Everolimus-Eluting Coronary Stent System

PROMUS Element is a device/drug combination product composed of two components, a device (coronary stent system including a platinum chromium stent platform) and a drug product (a formulation of everolimus contained in a polymer coating).

DRUG

Aspirin

Patients are required to take aspirin indefinitely after stent implant. It is recommended that aspirin 162-325 mg daily be given for at least 6 months after stent placement and that aspirin 75-162 mg daily be given indefinitely thereafter.

DRUG

Thienopyridine

Patients must be treated with one of the following thienopyridines for at least 6 months following the index procedure: clopidogrel 75 mg daily; or ticlopidine 250 mg twice daily; or prasugrel (outside the United States and if approved at the time of the procedure). If used, the prescribed dose should be in accordance with approved country-specific labeling. In patients not at high risk of bleeding, thienopyridine treatment should continue for at least 12 months after stent implant.

Trial Locations (5)

49770

Cardiac & Vascular Research Center of Northern Michigan, Petoskey

80538

Medical Center of the Rockies (Loveland), Loveland

Unknown

Saiseikai Yokohama-City Eastern Hospital, Yokohama

Sakakibara Heart Institute, Japan Research Promotion Society for Cardiovascular Diseases, Fuchu-shi

Tokyo Women's Medical University Hospital, Shinjuku-ku

Sponsors
All Listed Sponsors
lead

Boston Scientific Corporation

INDUSTRY