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临床试验/NCT02403297
NCT02403297终止不适用

Rapid Point-of-Care Salivary Diagnostic for Periodontal Health

Innovative Diagnostics Inc1 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2015年3月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
93
试验地点
1
主要终点
Presence of MMP-8 in the subjects saliva using the Quik Check PD device

研究概览

简要总结

The purpose of this study is to learn if a chair-side testing device will accurately measure levels of a salivary biomarker and thus indicate if a patient has periodontal health, gingivitis or periodontal disease.

详细描述

Human subjects will participate in this cross-sectional study by attending a single visit where their mouth will be examined and saliva will be collected to help determine the accuracy of a POC salivary diagnostic device. The study population will consist of 174 persons (58 that are orally healthy and have no oral discomfort; 58 that have gingivitis; and 58 that have periodontitis. The device results (i.e., visual and optical scans) will be compared against the Luminex results by two methods: 1) the Bland-Altman procedure and 2) discriminant analysis that examines whether the concentration would correctly identify the subject as health or disease using a defined threshold for MMP-8 levels.

Three groups of individuals will be recruited: those that are orally healthy and do not have any oral discomfort (N=58), those who have gingivitis (i.e., bleeding gums; N=58), and those who have periodontal disease (N=58). The groups will be matched by gender and smoking status. Women are predicted to account for 50% of the participants. The age distribution will be 18 to 95 years. Subjects will not be excluded based on race, gender, or ethnicity.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males or females of all racial and ethnic groups over 18 years of age;
  • At least 20 erupted teeth and the ability to provide expectorated saliva;
  • Able and willing to comply with study requirements; and
  • Have full understanding of all elements of, and signature and dating of the written informed consent prior to the initiation of protocol specified procedures

排除标准

  • Prisoners or institutionalized individuals;
  • Persons with acute illness or infectious disease (as evidenced by fever, malaise, sore throat, recurrent cough, lymphadenopathy, swelling and/or a physician consultation);
  • Evidence of oral mucosal lesion or ulceration; or
  • Use of glucocorticoids or cyclooxygenase inhibitors (i.e. such as ibuprofen, Naprosyn(Aleve) or non-steroidal anti-inflammatory drug) daily for the past two weeks.

结局指标

主要结局

Presence of MMP-8 in the subjects saliva using the Quik Check PD device

时间窗: One day. Subjects complete the study in 45 minutes.

次要结局

  • Amount of MMP-8 in the subjects saliva sample using Luminex Analysis(One day. Subjects complete the study in 45 minutes.)

研究者

发起方
Innovative Diagnostics Inc
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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