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临床试验/NCT01599442
NCT01599442终止不适用

Register for Patients With Diabetic Foot Syndrome and Critical Limb Ischemia

GWT-TUD GmbH1 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2010年6月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
GWT-TUD GmbH
入组人数
123
试验地点
1
主要终点
duration of survival without major amputation

研究概览

简要总结

Diabetic foot syndrome (DFS) is a disease caused by neurogenic (concerning the nervous system), vascular, mechanic and metabolic factors, which are further complicated by an impairment of the immune system and a corresponding increase in the risk for infections. Results from clinical trials about the efficacy of interventions aimed at reducing the number of patient-relevant end points are of limited comparability due to the heterogenity of patient characteristics. By their very nature, randomized clinical trials (RCT) can only focus on a limited section of the wide range of possible intervention regimes. In clinical practice, however, a number of patients with dfs will never have been part of a clinical trial. Furthermore, there are only very few contemporary registers for this indication from which conclusions with regard to the comparative merits of different therapeutic strategies may be drawn.

The register was conceived to find out to which extent RCT patients are representative for the overall patient collective with dfs and critical limb ischemia and to evaluate the therapeutic success of other treatment strategies. An RCT to assess the efficacy of urokinase versus placebo is imbedded in the register.

详细描述

August-1 is a register to find out to which extent RCT patients are representative for the overall patient collective with dfs and critical limb ischemia and to evaluate the therapeutic success of other treatment strategies. An RCT to assess the efficacy of urokinase versus placebo is imbedded in the register.

研究设计

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

入排标准

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

入选标准

  • diabetic patients with dfs and critical limb ischemia
  • age 18 and older

排除标准

  • less than 1 year life expectancy
  • prior major amputation
  • planned major expectation
  • prior treatment of the current episode of dfs with urokinase
  • mechanical heart valve replacement
  • cerebral event with changes in CT during the last three months
  • non-remediated proliferating retinopathy
  • uncontrolled hypertension (systolic > 180 mmHg, diastolic > 100 mmHg)
  • hemorrhagic diathesis (spontaneous quick value < 50%, spontaneous ptt > 40 sec, thrombocytes < 100 gpt/l)
  • acute gastrointestinal bleeding or ulcers during the last 4 weeks
  • prior reverse bypass operation
  • concomitant participation in other clinical trials
  • insufficient compliance
  • premenopausal women not using a safe method of contraception (i. e. IUD, hormone implants, hormone depot injection, combined pill (estrogens and gestagens), vaginal ring or vasectomized partner).

结局指标

主要结局

duration of survival without major amputation

时间窗: to be assessed after 12 months observation

次要结局

  • major amputation(after 12 months observation)
  • total mortality(after 12 months observation)

研究者

发起方
GWT-TUD GmbH
申办方类型
Other
责任方
Sponsor

研究点 (1)

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