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临床试验/NCT05647824
NCT05647824已完成不适用

User Performance of the TV4 Blood Glucose Monitoring System

Ascensia Diabetes Care3 个研究点 分布在 1 个国家目标入组 402 人开始时间: 2020年2月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
402
试验地点
3
主要终点
Fingerstick Test: Obtain TV4 BGMS performance data in the hands of lay users with diabetes using fingerstick capillary blood obtained with Microlet NEXT® lancing device.

研究概览

简要总结

Thunder V4 (TV4) is the code name of a blood glucose monitoring system (BGMS) consisting of a new meter and new Contour FIT test strips. This clinical trial will assess the performance (accuracy) of the TV4 meter by lay users enrolled as subjects in the study, and by health care professionals (also called study staff).

详细描述

The study will be conducted at three clinical sites and enroll a total of approximately 402 lay users. Ten to fifteen percent (10 - 15%) of the enrolled subjects will be naïve users (naïve to SMBG's and may include people without diabetes). At least twenty percent (20%) of subjects enrolled with diabetes will have Type 1 diabetes. At least 70% of subjects will be younger than age 65. Sites will also enroll subjects of Chinese descent.

This clinical investigation will be conducted within the US.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

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

入选标准

  • •Males and females, 18 years of age and older
  • •Ability to speak, read and understand English. Subjects must demonstrate the ability to read a paragraph from the first page of the User Guide (UG) to qualify for the study.
  • •Willing to complete all study procedures

排除标准

  • •Subjects without diabetes that are not naïve to Blood Glucose Monitoring System.
  • •Hemophilia or any other bleeding disorder
  • •Pregnancy (self-reported)
  • •Physical, visual or neurological impairments that would make the person unable to perform testing with the BGMS.
  • •Previous use of the Ascensia Contour Thunder V3 (TV3), or Thunder PLUS (T-PLUS), or Thunder V4 (TV4) BGMS.
  • •Working for a medical laboratory, hospital or another clinical setting that involves training on, or clinical use of blood glucose monitors.
  • •Being in this trial during or soon after xylose absorption testing (Xylose in the blood is known to cause interference). However, subjects can be enrolled as soon as 2 days after the test is performed (25 gms of oral xylose administered during this test is cleared within 480 mins or 8 hours).
  • •A condition, which in the opinion of the investigator or designee, would put the person or study conduct at risk. The reason for exclusion will be clearly documented by investigator or designee on the subject disposition form.
  • •Working for a competitive medical device company, or having an immediate family member or someone who is not a family member but is living within the household of someone who works for such a company.
  • •Immediate family members are the subject's parents, spouse, children, and siblings, including the parent's spouse; step-children and adopted children and their spouses.
  • •A competitive medical device company is a company that provides a medical device or components of a device that is related to diabetes.
  • •For example, people who are not eligible are those who work for companies that create or manufacture the following (or a company that is in a partnership with a company that provides such devices): lancing devices, blood glucose monitoring systems, continuous glucose monitoring systems, insulin pens, or systems related to the measurement of HbA1c.
  • •People who are eligible are those who work for companies associated with products such as wound dressings, medications or dietary products.

结局指标

主要结局

Fingerstick Test: Obtain TV4 BGMS performance data in the hands of lay users with diabetes using fingerstick capillary blood obtained with Microlet NEXT® lancing device.

时间窗: 4 weeks

Number of glucose results falling within ±15mg/dL of laboratory method at glucose concentration \<100 mg/dL and within ±15% at glucose concentrations ≥100 mg/dL

次要结局

  • Venous Blood Test: Obtain TV4 BGMS performance data using venous blood from lay users with diabetes.(4 weeks)
  • Alternative Site Test (AST): Obtain TV4 BGMS performance data in the hands of lay users with diabetes using capillary blood from the palm site obtained with Microlet NEXT lancing device with the AST endcap.(4 weeks)
  • Subject Questionnaire on the Usability of TV4 BGMS(4 weeks)

研究者

发起方
Ascensia Diabetes Care
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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