跳至主要内容
临床试验/NCT04933461
NCT04933461已完成不适用

Simulated Clinical Use Testing to Evaluate Sharps Injury Prevention Features of HTL-STREFA's Safety Lancets (Test C)

HTL-Strefa S.A.4 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2019年9月24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
20
试验地点
4
主要终点
The true failure rate of the tested devices.

研究概览

简要总结

A simulated clinical use testing to evaluate the Medlance Plus and myLance sharps injury prevention feature in accordance with the FDA's guidance on medical devices with sharps injury prevention features.

详细描述

This study aims to evaluate the safety of the use of the following safety lancets: Medlance Plus and myLance in the prevention of needle-stick injury (NSI) and to evaluate the user's opinion with regard to the handling characteristics of the medical devices.

The simulated use clinical study involves healthcare professionals (HCPs) who routinely use safety lancets to collect blood samples.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

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

  • evaluators who routinely use safety lancets to collect capillary blood samples (prevention of the learning curve artifacts)
  • evaluators will be United States (US) residents
  • evaluators can read, write, and speak English
  • evaluators are at least 18 years old
  • evaluators are able to understand and provide signed consent for the study
  • evaluators are willing to comply with the study protocol, including being willing to answer questions and complete questionnaires.
  • evaluators have no concerns about the ability to perform the simulated skin pricking.

排除标准

  • evaluators who do not routinely use safety lancets to collect capillary blood samples,
  • evaluators who cannot read, write, and speak English,
  • evaluators or a family member have a business or consulting relationship with a pharmaceutical or medical device company, or
  • evaluators who have participated in a product evaluation or marketing study involving safety lancets within the last six months

结局指标

主要结局

The true failure rate of the tested devices.

时间窗: At time of testing, up to 90 minutes

Effectiveness of the safety lancet's sharps injury prevention features.

时间窗: At time of testing, up to 90 minutes

Evaluator questionnaire using five-point response Likert scale (coded from 1 "strongly disagree" to 5 "strongly agree") to measure respondents' attitudes to a particular question or statement. Numbers assigned to Likert scale express a "greater than" relationship.

次要结局

  • Evaluation of various aspects of the ease of use.(At time of testing, up to 90 minutes ])
  • Evaluation of the safety of the devices based on the evaluators' assessments.(At time of testing, up to 90 minutes ])
  • Detection of any handling, usability questions / issues associated with the device.(At time of testing, up to 90 minutes ])

研究者

发起方
HTL-Strefa S.A.
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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