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临床试验/NCT06546579
NCT06546579招募中早期 1 期

Sensitivity of Self-collected Skin Sampling for Scabies: a Pilot Study

Radboud University Medical Center2 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2024年8月21日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
招募中
入组人数
144
试验地点
2
主要终点
The sensitivity of professionally-collected skin samples for diagnosing scabies

研究概览

简要总结

In this cross-sectional diagnostic study, healthy adults aged 18 and older with suspected, clinical, or confirmed scabies will be recruited. The objective is to determine if the sensitivity of self-collected skin samples for scabies diagnosis is non-inferior to professional sampling, and compare the sensitivity and specificity of the polymerase chain reaction assay (PCR) versus microscopy.

详细描述

Scabies infestations have significantly increased globally in the last 10-20 years, including a threefold rise in the Netherlands over the past decade. Diagnosing scabies is challenging due to varied symptoms and low sensitivity of current microscopic methods. New diagnostic techniques like PCR, which offer higher sensitivity, are being investigated. The feasibility of self-collected skin samples is being explored to reduce the burden on healthcare services and address issues like autonomy, stigma, and privacy.

In this cross-sectional diagnostic study, healthy adults aged 18 and older with suspected, clinical, or confirmed scabies will be included. Primary endpoint is the sensitivity of self-collected versus professional skin samples for diagnosing scabies. Secondary endpoints include sensitivity of skin scrapings and swabs, and the sensitivity and specificity of PCR versus microscopy.

Participants will self-collect skin samples during a standard care visit. The process may be slightly sensitive but not painful. There are no direct benefits beyond standard care.

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
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

  • 18 years or older
  • Have either suspected scabies, clinical scabies or confirmed scabies (see table 1)
  • Providing informed consent (IC)

排除标准

  • Individuals not speaking or understanding the Dutch or English language.
  • Individuals who have been diagnosed with scabies in the last six weeks and had started treatment.
  • Individuals who have used ivermectin for other diagnoses than scabies in the last six weeks.
  • Individuals younger than 18 years.
  • Individuals with immunosuppressive conditions (see appendix A).
  • Any other condition, finding or situation which, in the opinion of the investigator, may significantly increase the risk to the individual because of participation in the study, affect the ability of the individual to participate in the study or impair interpretation of the study data.

结局指标

主要结局

The sensitivity of professionally-collected skin samples for diagnosing scabies

时间窗: through study completion, an average of one year

The proportion of professionally-collected samples collected at the enrolment visit that are tested positive, divided by the total number of participants adjudged retrospectively to have had scabies at their enrolment visit, based on a composite clinical diagnosis.

The sensitivity of self-collected skin samples for diagnosing scabies

时间窗: through study completion, an average of one year

The proportion of self-collected samples collected at the enrolment visit that are tested positive, divided by the total number of participants adjudged retrospectively to have had scabies at their enrolment visit, based on a composite clinical diagnosis.

次要结局

  • The sensitivity of skin swabs for diagnosing scabies(through study completion, an average of one year)
  • The sensitivity of skin scrapings for diagnosing scabies(through study completion, an average of one year)
  • The sensitivity and specificity of PCR on skin scraping for diagnosing active scabies infection(through study completion)
  • The sensitivity and specificity of microscopy on skin scraping for diagnosing active scabies infection(through study completion, an average of one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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