Skip to content

Här är det bara att börja fylla på innehåll.

Instruktion

Jag har lagt till sidorna även i huvudmenyn så det är lättare för dig att nå sidorna. Det tar vi bara bort sedan när det är klart.

Nedan innehåll är en klon på den generella references sidan som finns idag.

Rooted in academic research

 Nevisense originated from research at Karolinska Institutet in Sweden. Today, the technology is supported by a growing body of clinical evidence and used in clinical practice, dermatological research, and product development worldwide. 

Backed by clinical evidence

Peer-reviewed publications support Nevisense's clinical performance in assessing melanoma and keratinocyte cancers. Studies conducted across Europe, the US, and Asia demonstrate its value across a range of clinical settings.

 

Improving diagnostic accuracy

Clinical studies show that Nevisense can increase sensitivity for melanoma detection and provide objective information alongside visual examination and dermoscopy. This additional support can help clinicians make more informed biopsy decisions, particularly when assessing suspicious or ambiguous lesions.

IMG_0805
Scibase_IMG_1707_Foto Liza Simonsson croped

Supporting research and innovation

Nevisense is increasingly used in academic studies focused on skin health, barrier function and the effects of dermatological treatments. Research groups value its repeatability, non-invasiveness and quantitative data output.

 

Used by leading institutions

Hospitals, dermatology clinics and research centers in Germany, the US and other countries have integrated Nevisense into their workflows – citing improved diagnostic decision-making and streamlined patient care.

Trusted by experts. Chosen for results.

"Nevisense essentially offers two key advantages: First, fewer unnecessary excisions. Second, in my experience, a detection rate of nearly 100%". 
Prof. Dr. Axel Hauschild
Photo.AxelHauschild.2022.jpg

Validated in the largest study of its kind

The clinical performance of Nevisense was validated in a pivotal prospective study involving 1,951 patients and 265 melanomas—the largest study of its kind conducted in melanoma detection. The study demonstrated 97% sensitivity and a 99% negative predictive value, providing robust evidence for the use of Nevisense as an adjunct to clinical and dermoscopic evaluation.

 

 

Scibase_utan_fonster_mobile
90+
Clinical Studies
FDACE +
Approved
500+
Clinics
Scibase_IMG_1099_Foto Liza Simonsson

Included in guidelines

Nevisense EIS technology is recognized in European and US clinical guidance as a complementary technology that can support the assessment of suspicious skin lesions.

 

German S1 Guideline

The first German guideline on imaging diagnostics for skin diseases describes EIS as a potentially valuable clinical decision-support tool for assessing melanocytic and keratinocytic lesions.
Read the guideline 

EADO Melanoma Guideline

The European melanoma guideline reports a sensitivity of 97.7% and describes EIS as a potentially useful complementary tool in clinical practice.
Read the guideline

US Expert Consensus

A US expert panel concluded that EIS can significantly enhance diagnostic assessment and clinical decision-making for clinically indeterminate pigmented lesions—including melanoma—with SORT Level A evidence.
Read the consensus report

NCCN Guidelines

The NCCN Guidelines identify EIS among the diagnostic-support technologies that may aid in detecting new primary melanoma, particularly in patients with numerous or clinically atypical nevi.
Visit NCCN

Get in touch  

Would you like to learn more about the clinical evidence behind Nevisense or how it can support your practice? Contact the SciBase team!