跳至主要内容
临床试验/NCT04550000
NCT04550000
已完成
不适用

A Multi-center Sample Collection Study in Patients With Suspected Melanoma Utilizing DermTech's Non-invasive Adhesive Patch Biopsy Kits

DermTech2 个研究点 分布在 1 个国家目标入组 652 人2019年3月1日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Melanoma (Skin)
发起方
DermTech
入组人数
652
试验地点
2
主要终点
Up to 1000 samples will be compared for gene expression analysis results compared to biopsy findings.
状态
已完成
最后更新
3年前

概览

简要总结

A multi-center sample collection study in patients presenting with pigmented lesion(s) suspicious for melanoma. All suspicious lesions should meet at least one of the "ABCDE" criteria.

详细描述

A multi-center sample collection study in patients presenting with pigmented lesion(s) suspicious for melanoma. All suspicious lesions should meet at least one of the "ABCDE" (asymmetry, border, color, diameter, evolving) criteria. Patients will be consented for the study and screened against the inclusion and exclusion criteria. Once the patient is determined to be acceptable for the study they will be assigned a unique patient number and tissue collection will begin. Tissue from the lesion will be collected using DermTech's non-invasive adhesive patch kit according to the instructions for use followed by surgical biopsy. Digital dermoscopy of the lesion is preferred but not required.

注册库
clinicaltrials.gov
开始日期
2019年3月1日
结束日期
2022年7月15日
最后更新
3年前
研究类型
Observational
性别
All

研究者

发起方
DermTech
责任方
Sponsor

入排标准

入选标准

  • Males and females at least 21 years of age
  • Have a pigmented lesion suspicious for melanoma the pigmented lesion meets at least one of the "ABCDE" criteria
  • The pigmented lesion mst be at least 3mm and not more than 16mm in diameter
  • Patient is willing to follow the start of care to test and treat the pigmented lesion as determined by the treating physician
  • Willing to have DermTech adhesive patch biopsies performed
  • Must be able to complete study procedures as required by the protocol
  • Willing to provide informed consent to participate in this trial

排除标准

  • Require a surgical biopsy or excision of the lesion of interest prior to the DermTech non-invasive patch biopsy(ies)
  • Has an ulcerated or bleeding lesion that could confound the biopsy results
  • Has a suspicious lesion(s) in an area that was previously surgically biopsied
  • Has a lesion that is classified as "clinically" evident melanoma appropriate for excision
  • The lesion to be sampled is on the mucosal surface, palmoplantar surface or other area where adhesive patch biopsies cannot be performed
  • Has a known sensitivity to adhesive patches
  • Any significant medical condition that would indicate an unreasonable risk to the patient or potential interference with the study
  • Lesion is in a location were sufficient removal of non-vellus hair cannot be achieved (e.g., scalp)
  • Suspected non-melanoma skin cancer
  • Patients with contraindication(s) to surgical biopsy -

结局指标

主要结局

Up to 1000 samples will be compared for gene expression analysis results compared to biopsy findings.

时间窗: Samples will be extracted and analyzed once up to 1000 samples have been collected and compared to surgical biopsy reports. Analysis results are expected in 2021

gene expression associated with melanoma vs non-melanoma compared to surgical biopsy

Up to 1000 samples will be compared to biopsy results for DNA mutations

时间窗: Samples will be extracted and analyzed once up to 1000 samples have been collected and compared to surgical reports and DNA mutation analysis. Analysis results are expected in 2021

Dna mutations associated with more aggressive forms of melanoma

研究点 (2)

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