Dermatologic Diseases Clinical Trial
Official title:
A Multicenter Sample Collection Study Utilizing DermTech's Non-invasive Adhesive Patch Biopsy Kits in Subjects With a Variety of Dermatologic Conditions
NCT number | NCT04668846 |
Other study ID # | 17-06 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | October 1, 2020 |
Est. completion date | December 15, 2023 |
Verified date | March 2022 |
Source | DermTech |
Contact | James Rock |
Phone | 18582052736 |
jrock[@]dermtech.com | |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This sample collection study will recruit subjects with a variety of skin conditions from up to 15 geographically dispersed sites in the United States. Skin samples will be collected with the DermTech Adhesive Patch Kit from both lesional and non-lesional skin. Subjects may also be asked to return at a future data for additional collections. Collected skin samples will be analyzed for gene expression information, DNA and the microbiome.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | December 15, 2023 |
Est. primary completion date | October 30, 2023 |
Accepts healthy volunteers | |
Gender | All |
Age group | 21 Years and older |
Eligibility | Inclusion Criteria: 1. Males and females at least 21 years of age; 2. Have a dermatologic condition of interesting including but not limited too; atopic dermatitis, atopic asthma, skin cancers (i.e., basal, and squamous carcinoma, melanoma, etc.), lupus, rheumatoid and psoriatic arthritis, gutate and plaque psoriasis, palmoplantar psoriasis, palmoplantar contact dermatitis, fungal infections and cutaneous T cell Lymphoma that can be non-invasively biopsied with DermTech's adhesive patch kit; 3. Willing to allow additional DermTech adhesive patch biopsies to be performed; and 4. Willing to provide informed consent to participate in this trial. Exclusion Criteria: 1. Required a surgical biopsy or excision prior to a PLA on that lesion of interest; 2. Has an ulcerated or bleeding lesion that could cofound the PLA results; 3. Has a suspicious lesion(s) in an area that was previously surgically biopsied; 4. Has an allergy to tape or latex rubber; and 5. Receipt of any investigational drug therapy within four weeks of study enrollment, or concurrent participation in another interventional clinical study deemed by the treating physician to potentially influence this study. |
Country | Name | City | State |
---|---|---|---|
United States | Skin Care Research, LLC | Boca Raton | Florida |
United States | Elizabeth S. Robinson, MD | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
DermTech |
United States,
Krueger G, Jansen B, Yao Z. Non-Invasive Gene Expression Analysis Assay for Psoriasis. Poster Presentation American Academy of Dermatology. March 2017.
Yao Z, Moy R, Allen T, Jansen B. An Adhesive Patch-Based Skin Biopsy Device for Molecular Diagnostics and Skin Microbiome Studies. J Drugs Dermatol. 2017 Oct 1;16(10):979-986. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gene Expression Analysis | To collect skin tissue from subjects with a variety of dermatologic conditions, both lesional and non-lesional areas to analyze for unique gene signatures | 24 months |
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