Dal-OUTCOMES Trial: Difference between revisions
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==Objective== | ==Objective== | ||
The objective of this trial is to study the effect of dalcetrapib on cardiovascular mortality and morbidity in patients with recent acute coronary syndrome in patients on statin therapy | |||
==Timeline== | |||
====Start Date==== | |||
April 1, 2008 | |||
== | ====End Date==== | ||
Ongoing | |||
==Methods== | ==Methods== | ||
* Phase III trial | |||
* A 72-week prospective, randomized, multicenter, placebo-controlled double-blind clinical trial that recuited 15,871 patients followed by a 12-week reversal phase . | |||
* Inclusion criteria: Patients older than 45 years, patients on any statin therapy at any dose, previous hospitalization for acute coronary syndrome, patients with no cardiac biomarker elevation but with ECG changes that were not presumed to be previously present, or evidence of obstructive coronary disease, patients with myocardial infarction who underwent percutaneous coronary intervention, and patients with symptomatic congestive heart failure but LVEF > 40%. | |||
* Exclusion criteria: Triglyceride level above 400 mg/dL, pregnant or breast-feeding females, females with child-bearing potential who are not on effective contraception, symptomatic congestive heart failure by end of run-in period, hemoglobin ≤ 10 g/dL at end of run-in period, uncontrolled hypertension (SBP ≥ 180 mmHg or DBP ≥ 110 mmHg), HbA1c > 10 on second visit, renal insufficiency with creatinine > 2.2 mg/dL or clinically apparent liver disease or liver function tests > 1.5 above upper normal limit at end of run-in period, CPK > 3 times upper normal limit at 2nd visit, use of other anti-lipidemic agents except Ezetimibe or fish oil, use of other medications that increase HDL-C, previous exposure to CETP inhibitors, malignancy within 3 years, short life expectancy, alcohol or drug abuse within 5 years, hypersensitivity reactions to trial medications of components in placebo, other significant clinical and investigational conditions that the investigator finds important. | |||
* Acute coronary syndrome defined as: Cardiac biomarkers above upper normal limits with symptoms of acute myocardial ischemia, ECG signs of ischemia that were not presumed to be present previously, or loss of viable myocardium on imaging. | |||
* Run-in period: 4-12 weeks | |||
* 2 arms of the study: dalcetrapib 600 mg daily or matching placebo. All patients should use any statin medication at any dose. | |||
* Randomization stratified according to country and whether cardiac biomarker levels are elevated or not. | |||
* Primary outcomes were defined as death from coronary heart disease, coronary events that are listed as myocardial infarction, unstable angina with evidence of acute myocardial ischemia, cardiac arrest with resuscitation, and stroke. | |||
* Secondary outcomes were defined as unexpected coronary revascularization that does not include restenosis revascularization, death from any cause, change of lipoprotein and inflammatory markers levels. | |||
==Results== | ==Results== | ||
Revision as of 12:26, 18 September 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Objective
The objective of this trial is to study the effect of dalcetrapib on cardiovascular mortality and morbidity in patients with recent acute coronary syndrome in patients on statin therapy
Timeline
Start Date
April 1, 2008
End Date
Ongoing
Methods
- Phase III trial
- A 72-week prospective, randomized, multicenter, placebo-controlled double-blind clinical trial that recuited 15,871 patients followed by a 12-week reversal phase .
- Inclusion criteria: Patients older than 45 years, patients on any statin therapy at any dose, previous hospitalization for acute coronary syndrome, patients with no cardiac biomarker elevation but with ECG changes that were not presumed to be previously present, or evidence of obstructive coronary disease, patients with myocardial infarction who underwent percutaneous coronary intervention, and patients with symptomatic congestive heart failure but LVEF > 40%.
- Exclusion criteria: Triglyceride level above 400 mg/dL, pregnant or breast-feeding females, females with child-bearing potential who are not on effective contraception, symptomatic congestive heart failure by end of run-in period, hemoglobin ≤ 10 g/dL at end of run-in period, uncontrolled hypertension (SBP ≥ 180 mmHg or DBP ≥ 110 mmHg), HbA1c > 10 on second visit, renal insufficiency with creatinine > 2.2 mg/dL or clinically apparent liver disease or liver function tests > 1.5 above upper normal limit at end of run-in period, CPK > 3 times upper normal limit at 2nd visit, use of other anti-lipidemic agents except Ezetimibe or fish oil, use of other medications that increase HDL-C, previous exposure to CETP inhibitors, malignancy within 3 years, short life expectancy, alcohol or drug abuse within 5 years, hypersensitivity reactions to trial medications of components in placebo, other significant clinical and investigational conditions that the investigator finds important.
- Acute coronary syndrome defined as: Cardiac biomarkers above upper normal limits with symptoms of acute myocardial ischemia, ECG signs of ischemia that were not presumed to be present previously, or loss of viable myocardium on imaging.
- Run-in period: 4-12 weeks
- 2 arms of the study: dalcetrapib 600 mg daily or matching placebo. All patients should use any statin medication at any dose.
- Randomization stratified according to country and whether cardiac biomarker levels are elevated or not.
- Primary outcomes were defined as death from coronary heart disease, coronary events that are listed as myocardial infarction, unstable angina with evidence of acute myocardial ischemia, cardiac arrest with resuscitation, and stroke.
- Secondary outcomes were defined as unexpected coronary revascularization that does not include restenosis revascularization, death from any cause, change of lipoprotein and inflammatory markers levels.