Actively Recruiting
Evaluation of Nevisense as Support Tool for the Diagnose of Keratinocyte Skin Cancer
Led by SciBase AB · Updated on 2024-12-11
150
Participants Needed
1
Research Sites
81 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective study to assess efficacy of the Nevisense device in identifying keratinocyte skin cancer (KC) in patients suspected of having skin cancer based on the initial physician's assessment. All skin lesions with a suspicion of Basal cell carcinoma (BCC), Invasive Squamos cell Carcinoma (iSCC), Bowen's disease (BD) or actinic keratosis (AK) and destined for excision or biopsy for further histopathological analysis will be considered for inclusion in the study.
CONDITIONS
Official Title
Evaluation of Nevisense as Support Tool for the Diagnose of Keratinocyte Skin Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients of any ethnicity aged 18 years or older
- Presence of skin lesions with uncertain diagnosis suspicious for keratinocyte skin cancer such as basal cell carcinoma, invasive squamous cell carcinoma, Bowen's disease, or actinic keratosis
- Lesions planned for excision or biopsy for histopathological analysis
You will not qualify if you...
- Metastases of recurrent lesions
- Lesions located on acral skin such as sole or palm
- Lesions on areas of scars, crusts, psoriasis, or similar skin conditions
- Lesions on hair-covered areas like scalp, beard, or moustache
- Lesions located on genitalia
- Lesions previously biopsied, surgically treated, or traumatized
- Lesions on mucosal surfaces
- Lesions with foreign matter such as tattoos or splinters
- Lesions on or near acute sunburn
- Lesions on skin surfaces that are not measurable such as those on stalks
- Lesions on skin surfaces that are not accessible such as inside ears or under nails
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CentroDerm
Wuppertal, Germany
Actively Recruiting
Research Team
P
Per Svedenhag
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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