跳至主要内容
临床试验/NCT01650831
NCT01650831已完成不适用

Clinical Study to Evaluate the Equivalence of the Modified BreathID Compared to Currently Approved BreathID System in Detection of H.Pylori Infection

Meridian Bioscience, Inc.2 个研究点 分布在 1 个国家目标入组 113 人开始时间: 2012年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
113
试验地点
2
主要终点
Percentage of Patients With Dichotomous (Presence/Absence of H.Pylori) Outcome Agreement in Diagnosis of H. Pylori

研究概览

简要总结

The purpose of this study is to confirm equivalence of a new generation breath analyzer (Modified BreathID) in its ability to detect H. pylori compared to the currently approved BreathID® System.

详细描述

The ¹³C-Urea Breath Test (UBT) is a non-invasive test for detecting the presence of Helicobacter pylori (H. pylori) infection by the organism's urease activity. In the presence of H. pylori, the ingestion of urea, labeled with the non-radioactive isotope 13C, results in production of labeled 13CO2, which can be quantified in expired breath. Each test is performed using a test kit consisting of a 13C-urea tablet and citrica powder to be dissolved in tap water ("13C-urea solution"). Before and after ingestion of the 13C-urea solution, samples of exhaled breath can be collected using a nasal cannula for real-time analysis and comparison to baseline concentrations. The patient's exhaled breath is analyzed and the ratio between 13CO2 and 12CO2 is computed. The patient is considered H. pylori positive when the difference between the ratios exceeds a predefined threshold (5 delta over baseline (DOB)). The current device marketed by Exalenz is large and costly. Exalenz has built a smaller, cheaper and more reliable new generation device for this application. Equivalence is being demonstrated in this study.

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
Single (Investigator)

入排标准

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

入选标准

  • Be at least 18 years of age
  • Present with clinical indication of H. pylori
  • Have the ability and willingness to sign the Informed Consent Form-

排除标准

  • Current serious disease
  • Participation in other trials
  • Antibiotics and/or Bismuth preparations for four (4) weeks prior to test
  • PPI or H2 blockers for two (2) weeks prior to test
  • Childbearing or breastfeeding women
  • Based on opinion of investigator, subject should not be enrolled in this trial
  • Allergy to citrus juice
  • Post -eradication therapy for H. pylori

结局指标

主要结局

Percentage of Patients With Dichotomous (Presence/Absence of H.Pylori) Outcome Agreement in Diagnosis of H. Pylori

时间窗: 25 minutes

The marketed (cleared) BreathID device and the investigational modified new generation BreathID device will measure simultaneously before (baseline) and after ingestion of substrate. The subject will be connected to both devices. The maximum time of measurement is 25 minutes.

Positive/Negative for H.Pylori With Cleared BreathID

时间窗: 1 hour

The amount of subjects that produced positive/negative results with cleared BreathID device

Positive/Negative for H.Pylori With Modified BreathID

时间窗: 1 hour

The amount of subjects that produced positive/negative results for H.pylori with modified BreathID

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)

Loading locations...

相似试验

Show Equivalence of the Modified BreathID Compared... | 临床试验