跳至主要内容
临床试验/EUCTR2011-002900-34-ES
EUCTR2011-002900-34-ES进行中(未招募)不适用

Population Pharmacokinetics in Benznidazol-treated adults with Chronic Chagas Disease. Benznidazol Pharmacokinetics and adverse reactions relationship. - Population Pharmacokinetics in Benznidazol-treated adults with Chronic Chagas Disease

CRESIB- International Research Center in Health of Barcelona0 个研究点开始时间: 2011年12月21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)
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

  • - Adult patients with Chronic Chagas Disease diagnosed by 2 different and positive serological tests.
  • - Patients with Chronic Chagas Disease who are going to start treatment with Benznidazol.
  • - Any gender.
  • - All the participants must agree to participate in the study and must sign the 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 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Patients yonger than 18.
  • - Patients with previous hipersensitivity to Benznidazol.
  • - Inmunocompromised patients as AIDS, cancer, chemoterapy, long-term corticoids need, primary inmunodeficiency, or any other.
  • - Hepatic dysfunction
  • - Renal dysfunction: serum creatinin higher than 3 mg/dl.
  • - Pregnancy or lactation.
  • - Low adhesion to treatment or check-up.
  • - Imposibility of follow-up.
  • - Severe adverse reaction to Benznidazol.
  • - Any other situation that could be risky for the patient.

研究者

发起方
CRESIB- International Research Center in Health of Barcelona

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