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临床试验/NCT03064087
NCT03064087进行中(未招募)不适用

Validation of Human Papillomavirus Assays and Collection Devices for HPV Testing on Self-samples and First-void Urine Samples (VALHUDES)

Marc Arbyn5 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2017年12月29日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
500
试验地点
5
主要终点
Clinical accuracy

研究概览

简要总结

The VALHUDES study is a Diagnostic Test Accuracy study that aims to document the clinical accuracy of hrHPV testing on urine samples, collected under standardised and optimised conditions, and on two types of vaginal self-samples and compare results with those from matching samples taken by a clinician.

详细描述

The samples are collected from patients referred to colposcopy because of prior cervical abnormalities. The patient takes at home two urine samples with the Colli-Pee device (a device that allows to collect first-void urine), the day before the visit to the colposcopy centre. At the colposcopy centre, two vaginal self-samples are taken by the patient herself: one with a cotton swab and a second with a plastic brush. Finally, the gynecologist takes a cervical Pap smear with a Cervex-Brush Combi.

A real-time PCR test will be used to detect DNA of high-risk HPV types. It is possible that in the future also other tests will be validated on these samples. The colposcopy and histological findings will be used as the gold standard. The main purpose of the study is to assess the relative diagnostic tests accuracy of hrHPV testing on self- and urine samples compared to hrHPV testing on cervical samples taken by a clinician. Furthermore, the participating women will receive also a questionnaire which can give insights into the attitudes and preferences of the women with regard to the self-sampling devices.

研究设计

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

入排标准

年龄范围
25 Years 至 64 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women with previous abnormal cervical cancer screening test results
  • Women between the ages of 25 and 64

排除标准

  • Hysterectomised women
  • Women with known pregnancy
  • Non-consenting women
  • Women that are not able to understand and to sign the informed consent

结局指标

主要结局

Clinical accuracy

时间窗: up to 18 months

• Relative sensitivity and specificity of hrHPV testing on vaginal self-samples vs clinician-collected samples.

次要结局

  • Clinical accuracy(up to 18 months)
  • Analytical performance(up to 18 months)
  • Acceptance and preferences(up to 18 months)

研究者

发起方
Marc Arbyn
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Marc Arbyn

Coordinator Unit Cancer Epidemiology (Belgian Cancer Centre)

Sciensano

研究点 (5)

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