Effects of Atorvastatin on Myonecrosis

PHASE4TerminatedINTERVENTIONAL
Enrollment

97

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

October 31, 2008

Study Completion Date

January 31, 2009

Conditions
Coronary Disease
Interventions
DRUG

Placebo Oral Tablet

placebo pre-PCI for ACS

DRUG

Atorvastatin 80mg

atorvastatin 80 mg pre-angio/PCI

OTHER

Screening

Patients signed consent to be screened for eligibility for randomization to placebo vs. study drug (atorvastatin)

Trial Locations (1)

02215

Beth Israel Deaconess Medical Center, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

Beth Israel Deaconess Medical Center

OTHER