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临床试验/NCT04542135
NCT04542135已完成2 期

Double-blind, Randomized Phase II Clinical Trial of Sulindac for Reducing Breast Density in Postmenopausal Women at Risk of Developing Breast Cancer

Alison Stopeck4 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2020年11月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
61
试验地点
4
主要终点
Change in percent breast density by MRI between treatment arms

研究概览

简要总结

The primary objective of this study is to determine if sulindac at a dose of 150 mg twice a day for 12 months reduces breast density in postmenopausal women at elevated risk of breast cancer when compared to a placebo control.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
35 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age ≤70 years
  • Subject must be postmenopausal.
  • Must have at least one healthy normal appearing breast (no prior diagnosis of invasive cancer, radiation or prosthetics). Prior biopsies are acceptable.
  • Must have dense breasts
  • Must be at elevated risk for developing breast cancer by abnormal pathological findings, family history, or genetic predisposition
  • A negative fecal occult blood test
  • Normal organ function
  • Hormonal therapy with aromatase inhibitors is allowed

排除标准

  • Daily aspirin or other daily anti inflammatory use.
  • Known intolerance to anti inflammatory.
  • Use of any selective estrogen receptor modulator therapy (e.g., tamoxifen, raloxifene) within past 12 months
  • Gastrointestinal, bleeding or coagulation, cardiovascular disorders.
  • Diabetes requiring insulin therapy.
  • Current regular smoker.
  • History of claustrophobia or inability to undergo imaging in a closed magnetic resonance imaging.
  • Cardiac pacemaker, cochlear implants, magnetic surgical clips or prostheses that would preclude MRI.
  • Uncontrolled hypertension.

研究组 & 干预措施

Sulindac

Active Comparator

sulindac 150 mg

干预措施: Sulindac Pill (Drug)

Placebo

Placebo Comparator

placebo pill

干预措施: Placebo (Drug)

结局指标

主要结局

Change in percent breast density by MRI between treatment arms

时间窗: 12 months

Change in Percent Breast Density by MRI Between Treatment Arms

时间窗: 12 months

The primary objective of this study is to determine if sulindac at a dose of 150 mg BID for 12 months reduces breast density in postmenopausal women at elevated risk of breast cancer when compared to a placebo control. The dependent variable is the relative change in percent breast density. Percent breast density is the estimated percentage of breast volume that appears dense versus fatty on the MRI, and relative change is calculated as the difference between the follow-up and baseline values divided by the baseline value.

次要结局

  • Change in percent breast density by MRI between treatment arms(6 months)
  • Changes in in percent breast density by MRI within and between treatment arms, stratified by use of aromatase inhibitors(12 months)
  • Change in Percent Breast Density by MRI Between Treatment Arms(6 months)
  • Changes in Percent Breast Density by MRI Within and Between Treatment Arms, Stratified by Use of Aromatase Inhibitors(12 months)

研究者

发起方
Alison Stopeck
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Alison Stopeck

Principal Investigator

Stony Brook University

研究点 (4)

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