跳至主要内容
临床试验/EUCTR2008-003249-10-DE
EUCTR2008-003249-10-DE进行中(未招募)不适用

Olmesartan, Oxidant Stress and in Vivo Re-Endothelialization Capacity of Endothelial Progenitor Cells from Patients with Chronic Kidney Disease (OECD Study) - OECD Study

niversity of the Saarland0 个研究点开始时间: 2009年2月11日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • * Signed written informed consent
  • * Woman or man aged 18 to 70 years
  • * Chronic Kidney Disease (CKD II-IV)
  • * Endogenous creatinine clearance between 15 ml/min and 90 ml/min. No impending need for dialysis during the study
  • * HbA1C <8% for patients with diabetes mellitus type II
  • * No Autosomal Dominant Polyzystic Kidney Disesase (ADPKD)
  • * No known metabolic diease except diabetes mellitus type II
  • 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

  • * Myelodysplastic or –proliferative diseases
  • * Malignant disease diagnosed within the last 5 years
  • * Renal anemia (Hb =10,5 g/dl for men or =10 g/dl for women) or therapy with rHuEPO or analogs
  • * Therapy with growth factors, e.g. GM-CSF or VEGF
  • * Statin Therapy
  • * Bleeding episodes relevant for Hb within the last 3 months or known gastrointestinal bleeding sources
  • * Foreseeable need for dialysis
  • * Sitting dBP >100 mmHg with standard antihypertensives (incl. ACE Inhibitors or ARB)
  • * Sitting sBP >100 mmHg with standard antihypertensives (incl. ACE Inhibitors or ARB)
  • * Known intolerance of ARBs, e.g. Olmetec®, Diovan®, Lorzaar®, Atacand®, Aprovel®, Mircardis®, Teveten®
  • * Known HIV infection
  • * Systemic chemotherapy or radiotherapy
  • * Chronic infection and/or CRP >10 mg/l at the beginning of the study
  • * Acute cardiovascular episodes
  • * Organ transplants
  • * Pregnant or lactating woman
  • * Woman of childbearing potential without adequate contraception
  • * Psychiatric disease or chronic cerebral attacks
  • * Non-compliance or participation in another clinical study within the last 30 days

研究者

发起方
niversity of the Saarland

相似试验