跳至主要内容
临床试验/PER-059-02
PER-059-02已完成未知

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 个研究点目标入组 0 人开始时间: 2002年9月4日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 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.

排除标准

  • 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

研究者

发起方
MERCK SHARP & DOHME PERU S.R.L.,

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