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临床试验/NCT04258449
NCT04258449招募中不适用

DOvEEgene Fleur: New Uterine Sampling Tool

McGill University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年12月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Patient related outcomes including pain and acceptability

研究概览

简要总结

This study is related to a previous study from the same group which started in 2014 (NTC02288676, McGill REB A08-M79-13B, MUHC REB 2020-5945) to develop a clinically implementable screening test -DovEEgene: developing and validating a novel molecular test for the early diagnosis of cancer of the endometrium, tubes and ovaries. This study is designed to identify endometrial, tubal and ovarian cancer very early based on identifying cancer-specific mutations (cancer DNA) in a pap sample taken from inside the uterus. The results are particularly encouraging given that control group is challenging with high background mutational burden from benign tumours, endometriosis, germ-line mutations etc.

To date, all the intrauterine samples were obtained using the commercially available TAO brush™ which is designed to take an endometrial sample. However, when patient tolerability was assessed using a numerical pain scale (NPS) ranging from 0 (no pain) to 10 (severe pain), patients rated the sampling using the TAO brush™ at 3.5 versus 0 for a cervical pap sample. These results were not surprising as the TAO brush™ was designed for dislodging strips of endometrial tissue to use for histopathologic examination. With respect to the investigators objective, which is to collect cancer cells that have exfoliated to the uterus, a sampler that collects these exfoliated cells with as little disturbance as possible to the underlying endometrium is preferred. In this sub-study, the investigators aim to evaluate a new endometrial sampling tool, the DOvEEgene Fleur, which is believe to be superior to the current TAO brush™ in terms of cancer detection, ease of use and patient tolerability. The sampler has been designed using materials/components found in the TAO brush™ and other approved medical devices.

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 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Be at least 18 years of age.
  • Have capacity to understand the study.
  • Be able to provide informed consent.
  • If the patient has a recently treated cervical abnormality, she must have had a Pap smear with normal results at least 4 months following treatment by loop electrosurgical excision procedure (LEEP) or cone biopsy.
  • Have suspected or confirmed cancer of the upper genital tract and be undergoing surgery for said tumor removal.

排除标准

  • Prior hysterectomy.
  • Be pregnant or possibly pregnant.
  • Be nursing, as the device contains phthalates (plasticizers) that "have not been fully characterized and there may be concern for reproductive and developmental effects".
  • Have an infected or inflamed cervix.
  • Have a confirmed or suspected pelvic infection.
  • Have a confirmed or suspected vaginal infection.
  • Have had recent history of uterine perforation.
  • Patients with recently treated cervical abnormalities must have a Pap smear with normal results at least 4 months following treatment by loop electrosurgical excision procedure (LEEP) or cone biopsy in order to be eligible.

结局指标

主要结局

Patient related outcomes including pain and acceptability

时间窗: up to 1 year

Evaluate pain tolerability and acceptability during and after endometrial sample collection. This will be assessed using pain scores reported by participants on numeric pain scale (NPS) ranging from 0 to 10. Final pain scores with the DOvEEgene Fleur will be compared to historical pain scores collected with the TAO brush (Cook Medical).

次要结局

  • Quality/quantity of sample collection(up to 1 year)
  • Feasibility of performing sample collection by clinicians(up to 1 year)

研究者

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

Dr. Lucy Gilbert

Professor Department of Obstetrics & Gynecology and Department of Oncology

McGill University

研究点 (1)

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