Skip to main content
Clinical Trials/PER-059-02
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

Sponsor
MERCK SHARP & DOHME PERU S.R.L.,

Similar Trials