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临床试验/PER-031-02
PER-031-02已完成未知

MULTICENTRIC, DOUBLE-BLIND, FOUR-PARALLEL GROUP, RANDOMIZED STUDY TO INVESTIGATE THE RESPONSE DOSE OF MICAFUNGIN (FK463) COMPARED WITH FLUCONAZOLE, ADMINISTERED TO HIV-POSITIVE PATIENTS WITH CONFIRMED CANDIDIASIS ESOPHAGITIS

FUJISAWAGMBH (ALEMANIA),0 个研究点目标入组 0 人开始时间: 2002年4月4日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 0(—)

入选标准

  • The patient must have candidiasis esophagitis, with or without involvement of the oropharyngeal area, without typical signs, documented clinical symptoms and confirmed by endoscopy. A histological / cytological confirmation should be obtained by brushing and esophageal biopsy, the results of which may still be pending at the moment of enrolling the patient.
  • Patient of both sexes older than 18 years.
  • The patient should have veins that are sufficiently accessible to allow medication to be administered.

排除标准

  • Evidence of liver disease.
  • Pregnant or breast-feeding patient.
  • Patient with significant renal disease.
  • Patient with another opportunistic disease.

研究者

发起方
FUJISAWAGMBH (ALEMANIA),

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