跳至主要内容
临床试验/NCT02441140
NCT02441140终止不适用

Detection of Tumor Associated Cell-free DNA in Peritoneal Fluid Obtained by Culdocentesis

Dana-Farber Cancer Institute4 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2015年5月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
5
试验地点
4
主要终点
Number of completed peritoneal fluid collection by culdocentesis after chromopertubation as an assessment of feasibility of peritoneal fluid collection in women with ovarian cancer.

研究概览

简要总结

This research study is studying a possible test which may help doctors diagnose women with ovarian cancer.

详细描述

This research study is a Feasibility Study, to try to evaluate whether or not culdocentesis can detect tumor associated cell free DNA. Although this is the first time investigators are using this type of procedure to detect cell free DNA, culdocentesis is not a new procedure. It used to be done routinely in the past to examine pelvic fluid. The investigator's goal is to develop a test to detect ovarian cancer in women before they develop any signs or symptoms of the disease. Currently, there is no screening test for ovarian cancer.

This study uses a technique called "culdocentesis" to detect DNA released by ovarian cancer cells into pelvic fluid. During culdocentesis, a small needle is inserted through the vagina into an empty space between the uterus and the rectum called the "cul-de-sac." Fluid is withdrawn from this space and sent for analysis. Culdocentesis is a technique that has been used for many years to examine pelvic fluid and determine its composition, but it has not previously been studied as a technique for examining cell-free DNA to detect ovarian cancer. The investigators suspect that this may be a useful way to detect cell-free DNA from ovarian cancer cells because the ovaries are very close to the cul-de-sac space.

In this study, the investigators will compare our ability to detect cell-free DNA in fluid from the cul-de-sac with our ability to detect cell-free DNA from a vaginal swab (similar to a Pap smear), a blood test, and in the tissue specimens collected at the time of surgery. The investigators are hoping to learn from this study whether developing a cell-free DNA test to screen for ovarian cancer involving culdocentesis would be an effective strategy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Able to give informed consent
  • Scheduled for surgery at Brigham and Women's Hospital for known or highly suspected Stage III or IV ovarian cancer (i.e. elevated CA-125 with a pelvic mass, ascites, and carcinomatosis)
  • Post-menopausal or negative urine and/or blood pregnancy test
  • Measurable disease on preoperative imaging

排除标准

  • Age < 18
  • Unable to give informed consent
  • Not planned for surgical intervention
  • Active malignancy other than ovarian cancer
  • Prior bilateral tubal ligation or hysterectomy (as this would prevent chromopertubation)
  • Known or suspected active pelvic infection
  • Pregnancy
  • No measurable disease or suspected Stage I or II ovarian cancer on preoperative imaging

结局指标

主要结局

Number of completed peritoneal fluid collection by culdocentesis after chromopertubation as an assessment of feasibility of peritoneal fluid collection in women with ovarian cancer.

时间窗: At the time of surgery

次要结局

  • Measure the concentration of cell free DNA in various biologic fluids and compare it to primary tumor DNA.(At the time of surgery)

研究者

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

Neil S. Horowitz, MD

Principal Investigator

Dana-Farber Cancer Institute

研究点 (4)

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