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临床试验/NCT02098226
NCT02098226Unknown不适用

Method Comparison Protocol: MALDI Biotyper-Clinical Applications (MBT-CA) Phase 2

Bruker Daltonics1 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
3,000
试验地点
1
主要终点
Substantial equivalence of MBT-CA with sequencing concerning determination of the respective bacteria and yeasts

研究概览

简要总结

The study objective is to confirm that the MBT-CA System identifies medically significant bacteria and yeasts from an isolated colony from any sample type processed by the clinical laboratory. For this purpose MBT-CA test results will be compared to bi-directional sequencing results.

详细描述

Bacteria or yeast isolates (1) fresh from primary culture plates, (2) collected directly from clinical samples, stored in the refrigerator or frozen or (3) well characterized organisms from a variety of contemporary culture collections will be included in the study. All organisms to be included in the study will be cultured on an agar medium prior to measurement.

Testing will be performed for various Gram negative and Gram positive bacteria and yeasts as outlined below. Several thousands of samples will be measured via MBT-CA systems based on MALDI-TOF MS technology (matrix assisted laser desorption ionisation time-of-flight mass spectrometry) at the test sites as fresh or frozen isolates of bacteria and yeasts. Lower prevalence organisms may be supplemented from banked culture collections.

The MBT-CA system uses an organism identification based on unique protein patterns of the microorganisms obtained from mass spectrometry. The test organism's spectrum (a pattern of mass peaks) is compared with a reference spectra library (database). Using biostatistical analysis, a probability ranking of the organism identification is generated. The probability ranking is represented as a log(score) between 0.00 and 3.00. Organism identification is reported with high confidence if the log(score) is ≥ 2.00. An organism identification is reported with low confidence if the log(score) is between 1.70 and <2.00.

In the last step the samples are sent to a special site for sequencing. Finally, the respective sequencing results are compared with the MBT-CA results.

Target microorganisms of study:

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with infections from certain yeasts, Gram positive or Gram negative bacteria (see Detailed Description)

排除标准

  • Patients without infections from the quoted microorganisms (see Detailed Description)

结局指标

主要结局

Substantial equivalence of MBT-CA with sequencing concerning determination of the respective bacteria and yeasts

时间窗: half a year

次要结局

未报告次要终点

研究者

发起方
Bruker Daltonics
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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