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Suction Based Characterization of Healthy and Diseased Skin

Mechanical Characterization of Healthy and Diseased Skin With Suction Based Assessment of Skin Deformability

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03644225
Enrollment
67
Registered
2018-08-23
Start date
2018-06-11
Completion date
2019-06-04
Last updated
2023-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic Sclerosis

Brief summary

The mechanical properties of healthy and SSc-diseased skin will be assessed by suction based measurements. The negative pressure needed to gain a certain tissue elevation, tissue elevation in response to a certain negative pressure as well as the time of retraction of tissue will be recorded and analyzed. Mesurments will be done with the new developed Aspiration Device\_Nimble and with the CE-certified Cutometer MPA 580.

Detailed description

Patients with systemic sclerosis (SSc) show a thickening of the skin due to massive deposition of collagen and temporary edema in the dermis. The clinical palpation method is currently the only diagnosis method. For an objective detection a non-invasive skin elasticity measurement can be performed. The widely used approach is based on local tissue suction. This study aims at an identification and quantification of mechanical and structural properties of human skin. The results will then be compared in age- and gender matched control groups. For evaluation of the skin elasticity measurement the results will be compared to the clinical parametar validated, modified Rodnan skin score (mRSS). The mechanical properties of healthy and diseased skin will be assessed by suction based measurements. The negative pressure is needed to gain a certain tissue elevation. Tissue elevation in response to a certain negative pressure as well as the time of retraction of tissue will be recorded and analyzed. (The different parameters depend on

Interventions

DEVICEMeasurment with Aspirational Medical Device

The mechanical properties of healthy and SSc-diseased skin will be assessed by suction based measurements with a new developed Aspirational Medical Device.

DEVICEMeasurment with Cutometer MPA 580

The mechanical properties of healthy and SSc-diseased skin will be assessed by CE-marked Cutometer MPA 580

Sponsors

Swiss Federal Institute of Technology
CollaboratorOTHER
Oliver Distler
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Masking description

No randomisation

Intervention model description

Primary outcome: Mechanical characterization of healthy and diseased skin using novel aspiration device and comparing it to the already validated Cutometer® MPA 580. Comparison of mechanical skin properties of healthy to patients' skin tissue (control vs. examined group). Secondary outcome: Defining predictors of the skin worsening.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

-Signed Informed Consent Healthy volunteers: \- Age ≥18 years old SSc-Patients: * Age ≥18 years old * Diagnosis of systemic sclerosis according to the ACR/EULAR 2013 criteria * Skin thickening diagnosed by clinical expert

Exclusion criteria

* Known or suspected non-compliance, drug or alcohol abuse, * Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant, * Previous enrolment into the current study, * Participants, who are unable to hold still * Impaired skin at the regions of measurements

Design outcomes

Primary

MeasureTime frameDescription
Mechanical characterization of healthy and diseased skin using novel aspiration device and comparing it to the already validated Cutometer® MPA 580.one visit, one measurement, one yearThe stiffness (mbar/mm) properties of healthy skin and SSc skin will be measured with the Aspiration Device and the Cutometer MPA 580. For comparison of different locations on the body, back of the hand (left and right) and dorsal forearm (left and right) will be assessed for every participant at one time point (Visite 1).

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026