D013493
Conditions
Keywords
Systemic sclerosis, firmness, skin evaluation, Rodnan score, mRSS
Brief summary
Systemic sclerosis (SSc) is an autoimmune disease characterized by skin fibrosis, which clinically manifests as thickening, hardening, and loss of elasticity of the skin. Patients are typically classified as having diffuse cutaneous SSc (dcSSc) or limited cutaneous SSc (lcSSc) depending on the extent of skin fibrosis. The standard assessment of cutaneous sclerosis is based on the modified Rodnan skin score (mRSS), which consists of clinical palpation of 17 areas of the body, scored from 0 (normal) to 3 (severe sclerosis) for each area, with a total of 51 points. However, the mRSS has several limitations, including high inter- and intra-observer variability, particularly depending on the clinician's experience, subjectivity of palpation with difficulties in quantifying subtle changes in firmness or elasticity, and limited sensitivity to small changes or in areas that are not severely affected. The assessment of skin fibrosis therefore faces a lack of objective, quantitative tools that are easy to use in routine clinical practice. Certain alternatives have been evaluated (durometer, ultrasound, elastography, etc.), but none has yet been fully adopted or validated for measuring firmness, elasticity, and adhesion at different depths of the skin with good accuracy and reproducibility. ADHELASKIN° technology (by Tactinnov, LTDS / École Centrale de Lyon) enables objective, highly sensitive measurement of rigidity, firmness and elasticity using an indentation method with a ruby ball sensor. The objective of our study is to assess whether the ADHELASKIN device can differentiate between the biomechanical properties of healthy patients and those of patients with SSc.
Interventions
DEVICEADHELASKIN (Tactinnov° - Ecole centrale de Lyon)
Evaluation of stiffness, elastic modulus and pile-up height for ScS patients and controls by ADHELASKIN device
Sponsors
Centre Hospitalier Universitaire de Saint Etienne
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients affiliated with or eligible for social security * Patients who have received informed consent about the study and have co-signed, with the investigator, a consent form to participate in the study * For case patients: Patients with SSc according to the 2013 ACR/EULAR criteria * For healthy patients: Patients without significant skin lesions who are outpatients or inpatients at a department of the Saint-Etienne University Hospital * For healthy volunteers: Volunteers without significant skin lesions who work at the Saint-Etienne University Hospital and whose participation in the study does not require any special travel
Exclusion criteria
* Persons deprived of their liberty, hospitalized without consent, hospitalized for purposes other than research; * Adults subject to legal protection measures (guardianship-curatorship) or unable to express their consent * Inflammatory or scarring dermatoses in different individuals
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Objectively compare skin stiffness in patients with systemic sclerosis versus healthy patients | Day 1 | General comparison of average stiffness values in Newtons per meter obtained using the ADHELASKIN device on all areas examined between affected and healthy patients |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Compare skin stiffness in different areas in patients with systemic sclerosis vs. healthy patients | Day 1 | Overall comparison of the sums and local averages and sums of the stiffness ( Newtons per meter) measured by the ADHELASKIN device on all areas explored between affected and healthy patients |
| Objectively compare skin elasticity in patients with systemic sclerosis vs. healthy patients. | Day 1 | Comparison of the overall and local averages and sums of the elasticity values measured by the ADHELASKIN device in kilopascals (kPA) |
| Objectively compare skin firmness in patients with systemic sclerosis vs. healthy patients. | Day 1 | Comparison of overall and local averages and sums of firmness values measured by the ADHELASKIN device in micrometers (μm) |
| Evaluate an association between the stiffness, elasticity, and firmness measurements obtained using the ADHELASKIN device and the mRSS score. | Day 1 | Correlation between skin thickening measured using the mRSS score by a trained investigator and biomechanical measurements of the skin measured by ADHELASKIN |
| Estimate the patient experience of skin assessment using ADHELASKIN | Day 1 | Standardized patient experience questionnaire in ScS and healthy patients. |
| Estimate inter-investigator variability in stiffness measurement using ADHELASKIN | Day 1 | Measurement of stiffness in N/m on a small cohort of 10 patients by 2 investigators using ADHELASKIN |
| Compare the duration of skin stiffness measurement examinations of 17 body regions by mRSS score and using ADHELASKIN | Day 1 | Measurement of the duration of the mRSS examination on the 17 regions and using the ADHELASKIN device on these same regions on 10 patients by a trained investigator |
Countries
France
Contacts
CONTACTLucile GRANGE, MD
CONTACTClara PFENNINGER, PhD
PRINCIPAL_INVESTIGATORLucile GRANGE, MD
Centre hospitalo-universitaire de Saint-Etienne
Outcome results
None listed