跳至主要内容
临床试验/NL-OMON53190
NL-OMON53190已完成不适用

METHOD CORRELATION OF SERUM, SODIUM CITRATE PLASMA, LITHIUM HEPARIN PLASMA AND K2-EDTA WHOLE BLOOD COLLECTED WITH VARIOUS COLLECTION TUBES AND COMPARED VIA SELECTED ICON CENTRAL LAB ASSAYS - Blood Sampling for Collection Tube Validation Study

ICON Clinical Research0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • 1. Sex : male or female; females may be of childbearing potential, of
  • nonchildbearing potential,
  • or postmenopausal.
  • 2. Age : 18 years or older, at screening.
  • 3. Body mass index (BMI) : 18.0 kg/m2 or higher, at screening
  • 4. Status : healthy subjects.
  • 5. Willing and able to sign the ICF.

排除标准

  • 1. Previous participation in this study
  • 2. Employee of ICON.
  • 3. Donation or loss of more than 450 mL of blood within 60 days prior to the
  • day of consent in the
  • current study.
  • 4. Significant and/or acute illness within 5 days prior to the day of consent
  • in the current study that
  • may impact safety, in the opinion of the Investigator.
  • 5. Unsuitable veins for blood sampling.
  • 6. Subjects who are, in the opinion of the Investigator, not suitable for
  • enrolment for another

研究者

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