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临床试验/EUCTR2006-000171-15-DE
EUCTR2006-000171-15-DE进行中(未招募)不适用

Randomized, placebo-controlled, double-blinded study evaluating the effects of Pioglitazone on intima-media-thickness (IMT) of the carotid arteries measured by MRI in non-diabetic patients with confirmed arteriosclerosis

niversity Hospital of Ulm0 个研究点开始时间: 2006年9月5日最近更新:
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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

  • Male or female patient at an age between 30 and 79 years (inclusive); the patient has a proven vascular disease defined as arteriosclerosis confirmed by the presence of CAD or PAD or carotid plaques; normal HbA1c (< 6%) plus normal fasting blood glucose (< 126 mg/dl) for 2 days prior to randomization (according to pre-study routine laboratory investigations); negative pregnancy test on Study Day 0 (Visit 1) in women with childbearing potential; signed and dated written informed consent
  • 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

  • Hemodynamic unstable patient or unstable acute coronary syndrome or state after acute myocardial infarction = 4 days; History of diabetes mellitus (any type 1 or 2); History of heart failure (NYHA I-IV) or relevant respiratory, renal (creatinine > 2.0 mg/dl), gastrointestinal or hematological diseases; History of renal failure requiring hemodialysis; Inadequate hepatic function (AST and ALT > 2.5 x ULN) ; History of severe/multiple allergies or systemic inflammatory diseases; History of any cancer disease or any cancer treatment in the last 5 years (exception: non-metastasizing skin cancer); Known/suspected hypersensitivity to pioglitazone or other TZDs; Pre- treatment with TZDs during 3 months prior to study enrolment; Severe claustro-phobia and/or MR-incompatible implants, and/or large sized coloured tattoos; Drug/alcohol abuse in the last 5 years; Blood donation in the last 30 days; Pregnant or nursing woman, or woman of childbearing potential not using effective contraceptive methods during the study (medications, patches, condoms, IUDs, male partner sterilization); Any further condition which according to the investigator results in an undue risk to the patient during participating in the present study

研究者

发起方
niversity Hospital of Ulm

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