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临床试验/EUCTR2005-003158-91-SE
EUCTR2005-003158-91-SE进行中(未招募)不适用

THE COLLABORATIVE STUDY GROUP TRIAL:THE EFFECT OF SULODEXIDE IN PATIENTS WITH TYPE 2 DIABETES AND MICROALBUMINURIA - Sulodexide in Type 2 Diabetes with Microalbuminuria

Keryx Biopharmaceuticals, Inc.0 个研究点目标入组 1,000 人开始时间: 2005年8月24日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • The principle inclusion criteria for the study includes men and women with type 2 diabetes and persistent microalbuminuria (in men urine albumin creatinine ratio [ACR] 35 – 200 mg albumin/G creatinine [4.0 - 22.6 mg/mmol], in women urine ACR 45 – 200 mg albumin/G creatinine [5.1 – 22.6 mg/mmol] based on the geometric mean of 3 first voided AM urine samples at the qualifying visit [Visit 6]). Patient’s serum creatinine must be ?1.5 mg/dL at screening.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Age of onset of type 2 diabetes <18 years;
  • 2.HbA1C >10.0%;
  • 3.Morbid obesity defined as a body mass index (BMI) ?45 kg/m2;
  • 4.Type 1 (insulin-dependent; juvenile onset) diabetes;
  • 5.Renal disease as follows:
  • Patients with known non-diabetic renal disease (nephrosclerosis superimposed on diabetic nephropathy acceptable);
  • Renal allograft;
  • 6.Absolute requirement for combination therapy of ACEI and ARB;
  • 7.Known allergies or intolerance to any heparin-like compound;
  • 8.Untreated urinary tract infection that would impact urinary protein values; or
  • 9.Prior exposure to sulodexide, either in a clinical setting or as a participant in another clinical study.

研究者

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