- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02808559
PASIMAT: Automatic Measure of PASI (PASIMAT)
June 17, 2016 updated by: Centre Hospitalier Universitaire de Nice
PASIMAT: Automatic Measure of PASI by Skin Imaging
To quantify the severity of psoriasis in a consistent and clinically meaningful way is important in order to decide the therapeutic orientation to take for the patient.
PASI (Psoriasis Area and Severity Index) scoring is recognised as gold standard for psoriasis assessment.
The bodystudio ATBM (Automatic Total Body Mapping) is a high-tech system performing standardized photos from head to feet and from all angles, which allows to map the entire skin covering all the human body in a few minutes.The primary objective of this study would be to evaluate the ability of the bodystudio ATBM to calculate the PASI score of patients with psoriasis human body in a few minutes
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Psoriasis is a chronic inflammatory skin condition resulting in a significant impact on patients' quality of life.
To quantify the severity of psoriasis in a consistent and clinically meaningful way is important in order to decide the therapeutic orientation to take for the patient.
PASI (Psoriasis Area and Severity Index) scoring is recognised as gold standard for psoriasis assessment.
However the measure of the PASI score is very complex.
Given this complexity, the PASI is influenced by inter and intra-rater variation.
In addition the PASI assessment process is time consuming.
The bodystudio ATBM (Automatic Total Body Mapping) is a high-tech system performing standardized photos from head to feet and from all angles, which allows to map the entire skin covering all the human body in a few minutes.
The mapping of the entire body is automatically done by the use of a digital camera performing 20 pictures of the patient with 8 successive positions.
The system is coupled to a software of automatic analysis of these pictures for the measure of the PASI score.
The primary objective of this study would be to evaluate the ability of the bodystudio ATBM to calculate the PASI score of patients with psoriasis
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age >= 18 years old
- Subject is affiliated to a National Health System at screening visit
- Understand and sign an Informed Consent Form (ICF) at screening, prior to any investigational procedures being performed.
- Patient with moderate to severe Plaque psoriasis.
- The patient is willing and able to be evaluated by the Bodystudio ATBM: 3 minutes for a young patient and until 7 minutes for an oldest.
- The patient is able to staying up during all the total body mapping procedure
Exclusion Criteria:
- The subject is vulnerable (such as deprived from freedom) as defined in Section 1.61 of International Conference on Harmonisation (ICH) Guideline for Good Clinical Practice (GCP).
- Pregnant woman or who are breast-feeding
- Patient with tattoos that could influence the PASI assessment.
- Patient with skin type (phototype) V or IV according to Fitzpatrick classification
- Male patients with exceeding facial or skin hair that could influence the automatic PASI assessment.
- Patients with exceeding varicose veins.
- Patients with sun burn
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Bodystudio ATBM
The PASI of the patients will be evaluated by two dermatologists then by the bodystudio ATBMs.
|
The mapping of the entire body is automatically done using a high-resolution apparatus (20 photographs of the patient in 8 positions (face, back, lateral left and right, specific extremities) The photographs will be done with a standardized procedure established by FotoFinder.
Every lesion is completely evaluated and the PASI score can be calculated.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Psoriasis Area and Severity Index
Time Frame: one day
|
one day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (Actual)
May 1, 2015
Study Completion (Actual)
May 1, 2015
Study Registration Dates
First Submitted
June 15, 2016
First Submitted That Met QC Criteria
June 17, 2016
First Posted (Estimate)
June 21, 2016
Study Record Updates
Last Update Posted (Estimate)
June 21, 2016
Last Update Submitted That Met QC Criteria
June 17, 2016
Last Verified
June 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14-AOI-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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