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临床试验/ISRCTN72526711
ISRCTN72526711已完成不适用

A randomized, open-labelled, parallel, comparative study of the efficacy and tolerability of rosuvastatin in low-density lipoprotein-cholestrol reduction using different dosing regimens of 5 mg daily, 10 mg daily and 10 mg on alternate days in Hong Kong Chinese type 2 diabetic patients

Chinese University of Hong Kong0 个研究点目标入组 120 人开始时间: 2006年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
120

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

性别
All

入选标准

  • 1. Type 2 diabetic patients 18 to 75 years of age
  • 2. Treated with diet alone, oral hypoglycemic agents and/or insulin
  • 3. LDL-Cholesterol >/= 2.6 mmol/l
  • 4. Dyslipidaemia persisting after diet control for eight weeks or more
  • 5. Alcohol consumption <50 g/day
  • 6. Not on treatment with drugs known to interfere with glucose tolerance or drugs that have a major effect on lipid metabolism e.g. thiazide diuretics and beta-blockers
  • 7. Good compliance to diet and drugs
  • 8. HbA1c <9% (glucosylated haemoglobin <9%)
  • 9. Blood pressure <160/95 mmHg

排除标准

  • 1. Significantly impaired renal function (plasma creatinine >150 micromol
  • 2. Impaired liver function (Serum Glutamic Pyruvic Transaminase [SGPT] or alanine aminotransferase [ALT] twice the upper limit of normal)
  • 3. Secondary dyslipidaemia, diabetic dyslipidaemia
  • 4. Pregnant women or those planning a pregnancy
  • 5. Lactation
  • 6. Progressive fatal disease
  • 7. History of drug or alcohol abuse
  • 8. History of hypersensitivity to study medication or drugs with a similar chemical structure
  • 9. Likelihood of requiring treatment during the study period with the following drugs: cyclosporine, erythromycin

研究者

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A randomized, open-labelled, parallel, comparative... | 临床试验