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临床试验/NCT01860963
NCT01860963已完成不适用

Prevalence of Anal Dysplasia in Patients With Inflammatory Bowel Disease and Healthy Controls

Stanford University2 个研究点 分布在 1 个国家目标入组 310 人开始时间: 2010年1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
310
试验地点
2
主要终点
Presence of high risk HPV and/or abnormal cytology

研究概览

简要总结

This study is designed to establish the prevalence of anal squamous intraepithelial lesion (ASIL) in patients with inflammatory bowel disease (IBD) and healthy controls.

详细描述

IBD patients attending the Stanford Inflammatory Bowel Disease (IBD) clinic and age-matched healthy controls are screened for eligibility. Informed consent is obtained for eligible subjects. An anonymous self-administered questionnaire is administered to assess risk factors for HPV. For IBD patients, information regarding IBD diagnosis and treatment is obtained.

An anal pap smear is performed at the time of a clinic visit or at the time of an already scheduled colonoscopy. Samples are collected and processed at Stanford pathology where a blinded pathologist reads all specimens. Human Papillomavirus (HPV) DNA testing is performed on all specimens. All patients with anal squamous intraepithelial lesion (ASIL) are referred to a colorectal surgeon for further recommendations or treatment, which includes a high-resolution anoscopy.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All IBD patients followed in the IBD clinic and healthy controls who are greater than 18 years old

排除标准

  • History of HPV vaccination
  • Pregnancy
  • Other immunosuppressed states (i.e. systemic lupus erythematosus, rheumatoid arthritis, cancer, Human Immunodeficiency Virus (HIV), transplant)
  • IBD patients who don't meet immunosuppression/non-immunosuppression criteria
  • Inability to obtain informed consent from patient
  • Previous diagnosis of ASIL or anal/rectal cancer

结局指标

主要结局

Presence of high risk HPV and/or abnormal cytology

时间窗: 1 day

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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