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临床试验/NCT00726856
NCT00726856已完成不适用

A Retrospective Survey to Evaluate the Effectiveness and Safety of Dual Inhibition Lipid-lowering Regimen in the Treatment of Dyslipidemic Patients in Normal Practice

Organon and Co0 个研究点目标入组 1,200 人开始时间: 2007年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
1,200
主要终点
Evaluation of the change in LDL-C levels after treatment

研究概览

简要总结

This retrospective study evaluates the effectiveness and safety of ezetimibe plus statin or ezetimibe plus fenofibrate in dyslipidemic patients that were treated with these dual inhibition lipid lowering regimens as part of their normal standard of care. This study assesses the percentage of patients who achieve LDL-C target goals and also evaluates the patient compliance to treatment.

详细描述

Retrospective medical chart review

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient was > 20 years and < 75 years of age on the index date*
  • Patient diagnosed with dyslipidemia who did not respond adequately based on NCEP ATP III target to previous lipid lowering treatment, and have received dual inhibition therapy, such as ezetimibe plus statins, ezetimibe plus fenofibrate or ezetimibe alone, for at least 3 months
  • Patient has at least one Total Cholesterol and LDL-C measurements at baseline and 3 months after initiating the dual inhibition therapy.
  • Patient has the following records documented in the chart during the data collection period:
  • Medical history and co morbidities (if available)
  • Total Cholesterol and LDL-C. test results before and after initiating the dual inhibition therapy
  • Prescription information of lipid-lowering dual inhibition regimens NOTE: * Index date: the date of initiating dual inhibition therapy

排除标准

  • Patients who do not meet all the inclusion criteria will be excluded from this survey.
  • Patients who were enrolled in other clinical trial observing specific study procedures which deviates from normal practice will not be included in this study.

研究组 & 干预措施

Patients

patients with dyslipidemia

干预措施: Ezetimibe 10 mg plus statin or ezetimibe 10 mg plus fenofibrate (Drug)

结局指标

主要结局

Evaluation of the change in LDL-C levels after treatment

时间窗: 3 months

次要结局

  • Assessment of the percentage of patients who attain their National Cholesterol Education Program (NCEP) Adult Treatment Panel (ATP) III target for LDL-C(3 months)
  • Assessment of patient compliance by evaluating the length of stay on therapy(3 months)
  • Comparison of the patient comorbidities among populations gathered from different levels of hospitals and specialties(3 months)
  • Evaluation of safety and tolerability in patients receiving dual inhibition therapy(3 months)

研究者

申办方类型
Industry
责任方
Sponsor

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