Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04491825
Other study ID # CTCL_Classifier_KLIF
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 22, 2021
Est. completion date June 30, 2024

Study information

Verified date April 2022
Source Medical University of Vienna
Contact Patrick M Brunner, MD, MSc
Phone +43140400
Email patrick.brunner@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Primary cutaneous T-cell lymphomas (CTCL) are a form of skin cancer that is derived from immune cells. The most common form of CTCL is mycosis fungoides (MF). While initially confined to the skin, MF may spread to lymph nodes, blood or inner organs, resulting in an overall poor prognosis for the patient. Thus, being a potentially lethal disease, an early and correct diagnosis of MF has very important implications for the patient. However, diagnosis of early MF is often difficult, as it usually shows a close resemblance to benign inflammatory conditions such as eczema and psoriasis. Strikingly, it takes an average of 3-6 (!) years from the appearance of the first skin lesions until a diagnosis of MF can be made. For this reason, a test to distinguishing early MF from benign inflammatory conditions is urgently mandated. By using skin suction blister fluid as well as skin biopsies from patients with MF, eczema and psoriasis, the investigators want to develop a classifier system that can distinguish early MF from benign inflammatory skin diseases.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date June 30, 2024
Est. primary completion date February 22, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Clinical and/or histopathological diagnosis of MF, eczema or psoriasis - Healthy control subjects without personal history of MF, eczema or psoriasis Exclusion Criteria: - Ongoing skin-targeted treatment (Wash out times: 2 weeks for topical, and 4 weeks for systemic treatments) - Ongoing other treatment that might, in the opinion of the investigator, influence proteomic features of the samples to be acquired

Study Design


Intervention

Diagnostic Test:
Skin suction blistering and skin biopsies
Skin suction blistering and skin biopsies will be used for the identification of potential proteomic biomarkers that can distinguish MF from eczema, psoriasis and healthy control skin.

Locations

Country Name City State
Austria Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proteomic signature of MF in comparison to eczema, psoriasis, and healthy control skin Proteomic multiplex assay At baseline