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
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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