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临床试验/NCT00703196
NCT00703196已完成2 期

HPV Clearance by Folic Acid Supplementation (FACT for HPV)

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 368 人开始时间: 2007年3月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
368
试验地点
2
主要终点
Clearance of HPV 16 and other coexisting HR-HPV and incidence of CIN ≥ 2

研究概览

简要总结

RATIONALE: Supplements, such as folic acid, may stop or delay the development of cervical cancer in women infected with human papillomavirus.

PURPOSE: This phase II trial is studying how well folic acid supplements work in preventing cancer in women infected with human papillomavirus.

详细描述

OBJECTIVES:

Primary

  • Evaluate the effects of folic acid supplementation on clearance of human papilloma virus (HPV) 16 and other specific types of HR-HPV and on prevention of the progression of ≤ cervical intraepithelial neoplasia (CIN) 1 lesions (not true preneoplastic lesions) to CIN ≥ 2 (true neoplastic lesions) by conducting a 12-month double-blind randomized placebo-controlled trial with 5 mg of folic acid/day.

Secondary

  • Evaluate whether the clearance of HPV 16 and other specific HR-HPV types and the progression of cervical lesions (≤ CIN 1 to CIN ≥ 2) is modified by lower levels of circulating and/or cervical cell folate, presence of micronuclei or global DNA hypomethylation in cervical cells, presence of integrated vs episomal HPV 16, or a high HPV 16 viral load in cervical cells at the enrollment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 120 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Clearance of HPV 16 and other coexisting HR-HPV and incidence of CIN ≥ 2

时间窗: One Year

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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