About this trial
Formation of a registry of IMID patients to assess the evolution of resistance to conventional and target therapies. This aim is achieved by evaluating the achievement of PASI 50 and PASI 75 scores at week 16 from the start of treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with a diagnosis of IMID.
Patients of any age, including minors.
Patients treated with approved medications for the condition in question and/or phototherapy.
Patients who agree to sign informed consent.
Disqualifiers
Patients without a diagnosis of IMID.
Patients who do not consent to sign informed consent.
Trial population
In this study (registry) will be included all IMID patients afferent to the UO of Dermatology of IRCCS Istituto Ortopedico Galeazzi for an estimated total of 5 years of recruitment.
Trial design
Case-only
Prospective
Treatments tested in this trial
Questionnaires
Other interventionThis is a collection of data from normal clinical routine: patients will be asked to record the assessments they undergo during their course of treatment, without changing clinical practice in any way. Data inherent to the following procedures will be collected: examinations, laboratory tests, imaging tests, questionnaires and rating scales.
Treatment groups
12
Treatment groupsSee each treatment group below.
Trial outcomes
Primary outcomes
Registry of ImmuNe-mediated inflammatory Diseases (IMIDs)
Formation of a registry of IMID patients to assess the evolution of resistance to conventional and target therapies.
Secondary outcomes
PASI 50
Assess attainment of PASI 50 score from the start of treatment to all follow-ups
PASI 75
Assess attainment of PASI 75 score from the start of treatment to all follow-ups
Other outcomes
Special populations
Quantification and monitoring of IMID patients belonging to "special populations". Special populations include: homeless, transgender, amputees, para and quadriplegics.
Sponsors and contacts
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