Microvascular Coronary Disease In Women: Impact Of Ranolazine

PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

April 30, 2007

Primary Completion Date

December 31, 2009

Study Completion Date

December 31, 2009

Conditions
Myocardial Ischemia
Interventions
DRUG

Ranolazine

500mg, orally twice daily for 2 weeks, assuming tolerance, followed by 1000mg orally twice daily for an additional 2 weeks. If the participant is unable to increase dose secondary to side effects, she will remain on 500mg twice daily for the second 2-week interval.

DRUG

Placebo

Placebo, 500mg, orally twice daily for 2 weeks, assuming tolerance, followed by 1000mg orally twice daily for an additional 2 weeks. If the participant is unable to increase dose secondary to side effects, she will remain on 500mg twice daily for the second 2-week interval.

Trial Locations (1)

90048

AHSP, Los Angeles

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

CV Therapeutics

INDUSTRY

lead

Cedars-Sinai Medical Center

OTHER