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临床试验/NCT06743737
NCT06743737招募中不适用

Sensitivity and Specificity Study of Electromedical Device Nexkin DSPT and Manual Measurement of Hives in Allergy Skin Prick Tests

Insel Gruppe AG, University Hospital Bern1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
200
试验地点
1
主要终点
Measurement of the histamine (positive control) wheal by healthcare professional

研究概览

简要总结

Skin prick tests (SPTs), or intraepidermal tests, are the first diagnostic approach for people with a suspected allergy. SPTs are very simple, safe and quick. They are cheap tests and are very useful as a screening test for allergy, especially in diseases like bronchial asthma, rhinoconjunctivitis, food/drug allergy and anaphylaxis. Together with the clinical history, SPTs allow to draw conclusions on allergies based on the sensitization pattern.

Nevertheless, the technique itself has evolved very little and continues to be performed entirely manually. This has a few drawbacks that limit the utility of the tests, in many cases limiting them to a purely qualitative assessment.

In comparison to standard practice (manual measurement), the digital skin test reading device Nexkin DSPT can provide the following benefits for project participants: Automates and digitizes the test reading, provides test results in digital format, reduces variability and subjectivity and greater consistency of diagnosis, reduces manual tasks allowing health professionals providing quantitative instead of qualitative results and avoiding potential human errors and allows a faster workflow, resulting in shorter patient visits.

The aim of this study is to validate the clinical utility of the electromedical skin test reading device Nexkin DSPT regarding its use in allergology clinics for the reading of skin prick allergy tests. The overall purpose of the study is to determine the sensitivity and specificity of skin prick tests (SPT) performed using the current practice of the fully manual SPT procedure and those performed using the Nexkin SPT DSPT (digital) procedure and to compare the sensitivity and specificity of both methods.

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

入选标准

  • Patients who will undergo skin prick tests with panels of aeroallergens and/or foods.
  • Over 18 years of age. The patient or their representative has given consent to participate in the study.
  • The patient must not have taken an antihistamine in the last 5 days.

排除标准

  • Patients who are evaluated by more than 40 prick tests. Patients who have taken an antihistamine within the previous 5 days. Patients who are being treated with antidepressants or other drugs with an antihistamine effect.
  • Patients who suffer severe atopic dermatitis with forearm involvement. Patients with dermographism. Patients who are evaluated by intradermal testing. Pregnant women or women suspected to be pregnant. Vulnerable patients

结局指标

主要结局

Measurement of the histamine (positive control) wheal by healthcare professional

时间窗: At enrollment

Measurement of the NaCl (negative control) wheal by healthcare professional

时间窗: At enrollment

Measurement of the histamine (positive control) wheal by digital device

时间窗: At enrollment

Measurement of the NaCl (negative control) wheal by digital device

时间窗: At enrollment

次要结局

  • Measure of the time involved in the complete reading and recording of the results(At enrollment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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