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临床试验/NCT00658190
NCT00658190已完成不适用

Internet-Based Cervical Cytology Screening Program

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 175 人开始时间: 2003年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
175
试验地点
2
主要终点
Cervical cytology abnormal cases

研究概览

简要总结

The purpose of this study is to assess whether a system that couples automated screening of Pap Tests with transmission of machine selected digital images, and review by cytologists at a remote location, performs to a clinically effective standard of accuracy.

详细描述

This clinical study uses the automated screening capabilities of the FocalPoint Primary Screening System (BD) for gynecologic cytology specimens (Pap tests) to allow for automated field of view (FOV) selection, digital image capture, and subsequent Internet-based transmission to a custom designed computer-based image reading station. The system utilizes liquid-based cytology preparations (ThinPrep, SurePath). In such a system, no skilled cytology human resources are necessary at the scanning site, and all expertise can be centralized. Pilot studies showed that the task was feasible to a clinically relevant standard of care. Phase 1 trials on preselected and seeded specimens confirmed this clinical standard. The phase 2 trials extend the concept to a prospectively enrolled population of patients from 2 sites (Walter Reed, Mass General) thereby testing the concept in a population of normal disease prevalence. The final phase 3 will be a larger study with intended use design, siting a screening device at the 121st Army Hospital in Korea and interpreting the specimen images in the US. In addition to the reading of the specimens, the system is designed to give immediate "loop closing" results back to each specimen's originating point immediate upon completion of the test.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Female presenting to clinic for a Pap test for any reason

排除标准

  • Prisoners
  • Mentally unable to provide informed consent

结局指标

主要结局

Cervical cytology abnormal cases

时间窗: At enrollment

Identification of abnormalities compared to the initial interpretation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David C. Wilbur, MD

Pathologist

Massachusetts General Hospital

研究点 (2)

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Internet-Based Cervical Cytology Screening Program | 临床试验