The Femscope Calm Collect Device to Obtain Cervical Cells for Cancer Screening
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 13
- 试验地点
- 2
- 主要终点
- Specimen Adequacy Using The Femscope Calm Collect Device vs. The Traditional Brush Method
研究概览
简要总结
The goal of this clinical trial is to determine if cervical cells collected by the Femscope Calm Collect Device in women (sex assigned at birth) of adult age are the same quality and quantity as the cervical cells collected by the traditional brush method for cervical cancer screening. The main questions it aims to answer are:
- Increase the number of women who get screened for cervical cancer.
- Improve patient acceptance of getting cervical screening on a routine basis.
- Decrease pain and discomfort for patients having a PAP smear procedure.
Participants will
- Have two vaginal exams to collect cervical cells.
- State decreased pain and discomfort for patients having a PAP smear procedure.
- The Femscope Calm Collect Device (FCCD) will be more comfortable for the patient as measured by a patient satisfaction survey comparing the FCCD and the traditional speculum method of obtaining cervical cells.
详细描述
The FemScope Calm Collect Device is a novel medical device intended for vaginal inspection, cervical cancer screening, rectal cancer screening, and discharge/cell retrieval. The device allows for increased comfort (emotionally and physically) to the patient while meeting the requirements of a genital exam.
The FemScope system includes a light and camera, enabling visualization of the vagina and cervix and display on a screen. It also provides brushing/retrieval means, allowing the provider to obtain necessary cervical cells for a pap smear, HPV, and specimens needed for sexually transmitted disease (STI) testing. The system will also allow the direct visualization of rectal tissue sampled for human papillomavirus/rectal cancer. The system is designed to replace the speculum, provide the tools needed to perform comprehensive pelvic and topical rectal exams, provide cervical cancer screens, and be cost-competitive with existing speculum and tissue swab systems. It is simple and easy to use. The device comprises a reusable base portion, a removable protective sleeve, and a single-use cell retrieval cap for improved cost-effectiveness.
This instrument will revolutionize women's health care, replacing the antiquated speculum examination with modern scopes like those used to visualize many other portions of the human body. Having the instrument designed to facilitate exams in the LGBTQIA community is sorely needed and will improve gynecologic and genital examinations in that community
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Device Feasibility
- 盲法
- None
盲法说明
All specimens collected will receive a randomized number so the pathologist is not aware of the samples collected by the traditional brush method (Pap smear) and the cells collected by the Femscope Calm Collect Device.
入排标准
- 年龄范围
- 21 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •- Healthy female ages 21-45 with female reproductive organs present at the time of study.
排除标准
- •Pregnancy
- •Menopausal
- •Age less than 21 years
- •Age of 46+ years
- •History of reproductive cancer
- •Hysterectomy
结局指标
主要结局
Specimen Adequacy Using The Femscope Calm Collect Device vs. The Traditional Brush Method
时间窗: 1 hour
Specimen adequacy will be assessed using the Bethesda System For Reporting Cervical Cytology. Specimens will be rated as Satisfactory or Unsatisfactory for evaluation. The presence/absence of a Endocervical/Transformation Zone (EC/TZ) component, partially obscuring blood, and inflammation are indicators the Pap test is satisfactory for evaluation.
Number of Participants Who Experienced Pain/Discomfort During The Femscope Calm Collect Procedure
时间窗: Immediately post-procedure
A binary (yes/no) assessment of whether the participant experienced pain or discomfort during the Femscope Calm Collect Procedure.
Number of Participants Who Experienced Pain/Discomfort During The Regular Pap Procedure
时间窗: Immediately post-procedure
A binary (yes/no) assessment of whether the participant experienced pain or discomfort during the regular Pap procedure
次要结局
未报告次要终点
研究者
Marilyn S Filter
Professor of Nursing, School of Nursing, The University of Michigan-Flint
University of Michigan
