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临床试验/NCT04607304
NCT04607304已完成不适用

ABCA2 GIRMS Analytical Validation Clinical Performance Study - Patient Sample Collection

Cairn Diagnostics2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2020年10月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
95
试验地点
2
主要终点
Percent agreement in diagnosis

研究概览

简要总结

The purpose of this study is to collect human breath samples for use in a validation study intended to demonstrate equivalent clinical performance measures of new ABCA2 GIRMS (Automated Breath Carbon Analyzer-2 Gas Isotope Ratio Mass Spectrometer) instruments to the currently FDA-approved ABCA GIRMS (Automated Breath Carbon Analyzer Gas Isotope Ratio Mass Spectrometer) system. ABCA GIRMS systems are used to analyze the ratio of 13CO2 to 12CO2 in patient breath samples during the GEBT (Gastric Emptying Breath Test) procedure.

详细描述

In this study the participants will be administered the FDA-approved GEBT test, which involves collecting breath samples prior to and after consumption of a non-radioactive carbon stable isotope (13C) labeled test meal. Breath samples will be collected at times consistent with FDA approved labeling. Participant's breath samples will be analyzed on the currently approved ABCA GIRMS and on the new ABCA2 GIRMS instruments. The values collected from both systems will be used to determine the clinical diagnostic agreement at each individual time points and percent agreement in diagnosis between the approved ABCA GIRMS and the new ABCA2 GIRMS.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males and females, 18-85 old at time of signing the informed consent form fro healthy and intended use population participants (i.e. symptomology of gastroparesis). Women of childbearing potential must not be pregnant at the time of GEBT administration.
  • Ability to eat test meal and provide breath samples

排除标准

  • History or physical exam suggestive of pathophysiologic disorders such as renal failure, chronic heart disease, chronic respiratory disease, liver disease or malabsorption syndrome
  • History of abdominal surgery except appendectomy
  • Use of any medications that may alter gastric motility within two days of the study
  • Use of narcotics or anticholinergics within two days of the study
  • Females on hormone replacement therapy other than birth control medications
  • Receipt of an investigational drug within 4 weeks of the study
  • Pregnancy
  • Intolerance or allergy to any component of Gastric Emptying Breath Test meal
  • History of neurologic or psychiatric disorders

结局指标

主要结局

Percent agreement in diagnosis

时间窗: Up to 7 days per participant

Diagnosis compared between the comparative method (ABCA GIRMS) and the candidate method (ABCA2 GIRMS) at each post meal timepoint and the overall diagnosis

Diagnostic agreement at each individual timepoints

时间窗: Up to 7 days per participant

Gastric emptying rates (kPCD) values compared between the validated ABCA GIRMS system and the new ABCA2 GIRMS systems for each GEBT post meal collection timepoint (45, 90, 120, 150, 180 and 240-minute timepoints) and the overall diagnosis

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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