PER-059-02Completed未知
MULTICENTRIC, DOUBLE-BLIND, FACTORIAL STUDY CONTROLLED WITH PLACEBO AND RANDOMIZED TO EVALUATE EFFICACY AND SAFETY IN THE ALTERATION OF LIPIDS OF THE EZETIMIBE / SIMVASTATIN MIXED TABLET IN PATIENTS WITH PRIMARY HYPERCHOLESTEROLEMIA
MERCK SHARP & DOHME PERU S.R.L.,0 sites0 target enrollmentStarted: September 4, 2002Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •a. Men or women> 18 and <80 years of age.
- •b. People willing to make a regimen of Therapeutic Changes of
- •Lifestyle (TLC) of the NCEP or a similar diet of cholesterol reduction during the course of the study.
Exclusion Criteria
- •a. Weight <50% of the ideal body weight according to the Weight and Height Tables
- •Metropolitans of 1983 (Appendix 2) or weighing <100 pounds (45 kg).
- •b. Hypersensitivity to HMG.-CoA reductase inhibitors.
- •c. Patients who already receive lipid reduction therapy in which the
- •suspension of therapy for the course of the study would be inappropriate to
- •the investigator´s judgment.
- •d. Alcohol consumption> 14 drinks per week.
- •e. Pregnant women or breastfeeding
Investigators
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