跳至主要内容
临床试验/NCT06810427
NCT06810427进行中(未招募)不适用

A Novel, Low-Cost, Handheld 3D Imaging System for Improved Screening for Cervical Neoplasia in Resource-Limited Settings

Carilion Clinic1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2025年1月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
18
试验地点
1
主要终点
Image Quality and Resolution vs Standard-of-Care

研究概览

简要总结

The purpose of this study is to evaluate the design and engineering of a new minimally invasive medical imaging device (CervImage™). Investigators are trying to find out if CervImage™ is reliable and easy to use to obtain clinical 3D photographs and to record 3D measurements in human cervixes. Investigators then plan to use these images to determine if CervImage™ design and engineering improvements need to be made.

详细描述

This study intends to evaluate the design and engineering of an innovative, minimally invasive, 3D, and medical imaging device (CervImage™) for detecting cervical lesions. The research procedure and evaluation will be incorporated into the scheduled annual pap smear exam or colposcopic gynecologic exam that involves using a vaginal speculum. The CervImage™ camera will be positioned within the speculum approximately 1-2 cm distal to the cervix. It will not come into physical contact with the participant. Data collection with the CervImage TM imaging device is expected to take less than 5 minutes. The study will generate live cervical images and gather qualitative feedback from both clinicians and participants. CervImage™ is not a diagnostic product, and this study will not be generating any efficacy or imaging data to be used for diagnostic or therapeutic purposes. If any abnormalities are observed in the CervImage™ procedure described, they will be further evaluated by the Principal Investigator. This will take place during the participant's routine gynecologic exam with colposcopy included as part of their scheduled clinical visit. The device will not be used for diagnostic purposes or for making any clinical decisions or recommendations.

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

入排标准

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

入选标准

  • Patient 21 to 70 years of age at screening
  • Patients with known HPV infection or cervical intraepithelial neoplasia (16 patients)
  • Healthy patients without history of HPV/CIN (2 patients)
  • Participants able to consent for themselves

排除标准

  • Cognitive Impairment
  • Currently Pregnant
  • Incarcerated Individual
  • Any condition which in the clinical judgement of the PI makes the subject unsuitable or unsafe for study enrollment

研究组 & 干预措施

CervImage Device

Experimental

CervImage device for cervical imaging to detect cervical intraepithelial dysplasia [CIN] via colposcopy

干预措施: CervImage device (Device)

结局指标

主要结局

Image Quality and Resolution vs Standard-of-Care

时间窗: Immediately after the procedure

CervImage images evaluated on Spatial resolution, distortion, brightness, magnification, color correctness, corrupted pixel rows, and visual inspection vs standard-of-care cervical imaging for intraepithelial dysplasia \[CIN\] visualization.

次要结局

  • Time to Obtain Images(Immediately after the procedure)
  • Comfort/Discomfort of Subject(Immediately after the procedure)
  • Physician Satisfaction(Immediately after the procedure)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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