跳至主要内容
临床试验/NL-OMON40398
NL-OMON40398已完成4 期

Anidulafungin pharmacokinetics given as a single intravenous dose to obese patients (ADOPT). - ADOPT

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 8 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
8

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
18 至 99(—)

入选标准

  • 1. Patient has a BMI >=40 kg/m2 and is undergoing bariatric surgery.
  • 2. Subject is at least 18 years of age on the day of screening.
  • 3. If subject is female: neither pregnant, nor able to become pregnant and is not nursing an infant.
  • 4. Subject or legal representatives are able and willing to sign the Informed Consent before screening evaluations.

排除标准

  • 1. Documented history of sensitivity to medicinal products or excipients similar to those found in the anidulafungin preparation.
  • 2. History of or current abuse of drugs, alcohol or solvents.
  • 3. Inability to understand the nature of the trial and the procedures required.

研究者

发起方
niversitair Medisch Centrum Sint Radboud

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