Main characteristics of the included studies
| Trial |
Treatments |
Patients |
Methods |
MERLIN TIMI 36, 2007
NCT00099788
|
ranolazine 1000 mg twice daily for the duration of the trial (intitialy 200 mg intravenously for 1 hour, followed by an 80 mg/h intravenous infusion)
versus
placebo
|
Hospitalized with NSTE-ACS; ischemic symptoms at rest within 48 hours; and at least one indicator of moderate to high risk, defined as elevated troponin or creatine kinase-myocardial band, ST-depression >0.1 mV, diabetes, or TIMI risk score for unstable angina/NSTEMI >=3
|
follow-up median 11.4 months
n=3279/3281
Parallel groups
Double blind
17 countries
|
References
MERLIN TIMI 36, 2007 :
Morrow DEvaluation of a novel anti-ischemic agent in acute coronary syndromes: the primary results of the metabolic efficiency with ranolazine for less ischemia in non-ST elevation acute coronary syndrome (MERLIN)-TIMI 26 trial
American College of Cardiology Annual Scientific Session, New Orleans, LA, March 2007
[PMID ]
MERLIN TIMI 36, 2007 :
Morrow DA, Scirica BM, Karwatowska-Prokopczuk E, Murphy SA, Budaj A, Varshavsky S, Wolff AA, Skene A, McCabe CH, Braunwald EEffects of ranolazine on recurrent cardiovascular events in patients with non-ST-elevation acute coronary syndromes: the MERLIN-TIMI 36 randomized trial.
JAMA 2007 Apr 25;297:1775-83
[PMID 17456819]