NCT05172284Not yet recruitingNot Applicable
Registry and Monitoring of ImmuNe-mediated Inflammatory Diseases (IMIDs) REMIND Study
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio1 site in 1 country2,000 target enrollmentStarted: February 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 2,000
- Locations
- 1
- Primary Endpoint
- Registry of ImmuNe-mediated inflammatory Diseases (IMIDs)
Study Overview
Brief Summary
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.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •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.
Exclusion Criteria
- •Patients without a diagnosis of IMID.
- •Patients who do not consent to sign informed consent.
Outcomes
Primary Outcomes
Registry of ImmuNe-mediated inflammatory Diseases (IMIDs)
Time Frame: 15 years
Formation of a registry of IMID patients to assess the evolution of resistance to conventional and target therapies.
Secondary Outcomes
- PASI 75(15 years)
- PASI 50(15 years)
Investigators
Study Sites (1)
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