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AzTrials

Systemic Autoinflammatory Diseases (SAID)SHENCT07889960

Development of a Cloud Platform for Advanced Diagnostics Based on Clinical and Omics Data.

An observational study of Systemic Autoinflammatory Diseases (SAID) and Fibromyalgia, run by Istituto Giannina Gaslini at 3 sites in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims to explore how information from different types of biological tests, such as genetic, protein, and fat-related analyses, can help doctors better identify and distinguish patients with systemic autoinflammatory diseases (SAIDs), including undifferentiated or complex forms of these conditions (uSAIDs and… Read more about this study

Who is it for?
Ages Up to 25 years
How many people
73 participants
Where
3 sitesItaly
Study dates
12 Mar 2025to 31 Oct 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 25 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: Male and female subjects 0-25 years

Who may be able to join

  • Age 0-25 years.
  • Newly diagnosed active disease or unstable disease (ongoing attacks despite treatment), whether genetically confirmed or still undiagnosed.
  • The patient or their legal representative provides informed consent to participate in the study, including undergoing omics analyses and agreeing to the sharing and use of their clinical and omics data for subsequent analyses.
  • Monogenic SAID: Patients with clinical and genetic findings consistent with a monogenic SAID belonging to one of the following categories: inflammasomopathies, unfolded protein response (UPR) and cellular stress disorders, type I interferonopathies, actinopathies, NF-κB hyperactivation disorders, or DADA2. Physician Global Assessment (PGA) > 2 on a 0-10 visual analogue scale (VAS) and elevated C-reactive protein (CRP) levels.
  • Multifactorial/complex SAID: Patients with clinical manifestations consistent with PFAPA, SURF (as defined in Papa R et al., 2020), chronic recurrent multifocal osteomyelitis (CRMO)/SAPHO syndrome, or systemic juvenile idiopathic arthritis (sJIA). PGA > 2 on a 0-10 VAS and elevated CRP levels.
  • Undifferentiated SAID (uSAID): Patients with clinical manifestations consistent with a SAID, after exclusion of defined monogenic or multifactorial/complex autoinflammatory diseases based on clinical and/or genetic findings. PGA > 2 on a 0-10 VAS and elevated CRP levels.
  • Fibromyalgia (FM): Widespread pain with symptoms present for at least 3 months. Patients meeting the clinical criteria defined in Wolfe et al. (2016).

Who cannot join

  • Inflammatory bowel diseases or other inflammatory conditions that may mimic SAIDs (e.g., haematological disorders, malignancies, and immunodeficiencies).

Trial locations and contacts

3 sites in 1 country.

Italy3 sites
  • Engineering D.HUB (EDH)

    Aosta

  • IRCCS Istituto Giannina Gaslini

    Genova

  • Istituto Italiano di Tecnologia (IIT)

    Genova

Other trials in Italy

About this study

Official title: Development of a Cloud Platform for Advanced Diagnostics Based on Clinical and Omics Data - Sviluppo di Una Piattaforma Cloud Per la Diagnostica Avanzata Basata su Dati Clinico-omici

This study aims to explore how information from different types of biological tests, such as genetic, protein, and fat-related analyses, can help doctors better identify and distinguish patients with systemic autoinflammatory diseases (SAIDs), including undifferentiated or complex forms of these conditions (uSAIDs and SAIDs), as well as fibromyalgia. The goal is to improve diagnosis and help identify the most appropriate treatments and care options for each patient.

The study will also develop computer-based tools to identify important biological patterns in patients' medical records and laboratory results. These tools will help doctors interpret each patient's individual case and better understand their condition.

Finally, the study will bring together biological test results, clinical information, and the findings from these analyses in a single, comprehensive health record. This record will have an easy-to-use interface designed to support patients' care teams. Its usefulness in everyday clinical practice will then be evaluated.

Read the detailed description

Study Summary This is an open-label, multicentre, observational cohort study involving both retrospective and prospective collection of clinical data and biological samples.

Rare diseases represent a major healthcare challenge. Approximately 80% of currently known rare diseases are genetic in origin. These conditions are often complex, affect multiple organ systems, and are associated with significant morbidity, mortality, and healthcare costs. Reaching a correct diagnosis can take several years.

Systemic autoinflammatory diseases (SAIDs) are a growing group of rare disorders caused by dysfunction of the innate immune system. This dysfunction leads to recurrent or persistent episodes of sterile systemic inflammation, driven by the excessive production of inflammatory molecules called cytokines, including IL-1, IL-18, IL-6, TNF-α, and type I interferons. SAIDs may be rare or ultra-rare, but collectively they affect more than two million people in Europe. Up to 47 distinct disease entities have been identified, with both specific and overlapping clinical features.

Most autoinflammatory diseases have a strong genetic component, often involving mutations in a single gene. For known monogenic SAIDs, accurate disease classification is essential for selecting effective treatment. However, in approximately 40-60% of suspected cases, genetic testing does not provide a definitive diagnosis. These cases are classified as undifferentiated SAIDs (uSAIDs). Diagnostic uncertainty may delay appropriate treatment and increase the risk of irreversible organ damage. Undifferentiated cases may have a polygenic, multifactorial, or complex origin, with environmental factors also contributing to disease development and prognosis. Other conditions of interest in this study include systemic juvenile idiopathic arthritis (sJIA) and fibromyalgia (FMG).

Evidence suggests that patients with undifferentiated and complex SAIDs may benefit from personalised, stratified approaches to diagnosis and treatment, similar to those already used for some monogenic diseases. Achieving this requires the development of multi-omics profiles and artificial intelligence tools suitable for clinical practice.

Omics data are obtained by analysing groups of biological molecules, such as ions, nucleic acids, proteins, and enzymes, in samples including blood serum, urine, cerebrospinal fluid, saliva, and tissues. Different approaches, such as genomics, proteomics, and lipidomics, provide complementary information about how biological systems function. Integrating these data can improve understanding of disease mechanisms, natural history, prognosis, and treatment response.

However, interpreting molecular findings and combining them with clinical information remains challenging, particularly for rare diseases or cases in which the underlying cause is unknown. Although electronic health records (EHRs) are widely used in hospitals, omics data are rarely integrated into these systems. Clinical information is often shared with specialists through verbal communication or separate tools, such as email, rather than through a unified platform. This fragmentation can reduce efficiency, increase the risk of incomplete or inaccurate information exchange, and limit the reuse of data for future investigations. Identifying patients with similar clinical and genetic characteristics also often depends on the experience and memory of individual healthcare professionals.

This study aims to address these limitations by improving the speed, efficiency, and reliability of collaboration between clinical teams and specialists or organisations providing genomic and other molecular testing services.

Study Objectives

The study has three main objectives:

Improve diagnosis and patient stratification. Investigate whether omics data, including genomics, proteomics, and lipidomics, can help distinguish and classify patients with SAIDs, particularly undifferentiated and complex SAIDs, sJIA, and fibromyalgia. The ultimate goal is to support more accurate diagnoses and help identify the most appropriate treatments and care strategies for each patient.

Develop analytical algorithms and predictive models. Create computational tools capable of identifying relevant biological information in clinical and omics data and generating models to support the interpretation of individual patient cases.

Integrate clinical and molecular information. Develop a comprehensive, user-friendly clinical and omics record that combines patients' clinical histories, laboratory findings, omics data, and analytical results. Its usefulness in supporting patient care will then be evaluated.

The study will use leftover blood samples collected during routine laboratory testing, DNA samples already extracted for diagnostic genetic investigations, and, where available, previously collected and stored DNA, RNA, and serum samples held in the biobanks and repositories of the Istituto Giannina Gaslini. Clinical information will include data routinely collected to document patients' medical histories and current clinical conditions.

Expected Outcomes and Clinical Applications The project will develop an innovative clinical and omics electronic health record capable of systematically managing both conventional clinical information, including patient characteristics and medical history, and results from molecular investigations.

The platform will support searches of external databases and provide advanced ways to access and interpret patient information. It will also incorporate clinical decision-support functions to provide useful information to healthcare professionals and assist them in making informed decisions.

In addition, the project will develop computational pipelines to process raw genomic data and establish primary and secondary analysis protocols for omics data. These procedures will generate standardised results suitable for integration into the patient's electronic health record.

Overall, the project aims to improve the integration and interpretation of clinical and molecular information, facilitate collaboration between healthcare professionals and laboratory specialists, and support more timely, accurate, and personalised diagnosis and treatment for patients with rare and complex inflammatory conditions.

Medical subject headings
Fibromyalgia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07889960
Study groupRoleWhat they receive
monogenic SAIDPatients with clinical and genetic findings consistent with a monogenic SAID belonging to one of the following categories: inflammasomopathies, unfolded protein response (UPR) and cellular stress disorders, type I interferonopathies, actinopathies, NF-κB hyperactivation disorders, or DADA2. Physician Global Assessment (PGA) > 2 on a 0-10 visual analogue scale (VAS) and elevated C-reactive protein (CRP) levels.
Multifactorial/complex SAIDPatients with clinical manifestations consistent with PFAPA, SURF (as defined in Papa R et al., 2020), chronic recurrent multifocal osteomyelitis (CRMO)/SAPHO syndrome, or systemic juvenile idiopathic arthritis (sJIA). Physician Global Assessment (PGA) > 2 on a 0-10 visual analogue scale (VAS) and elevated C-reactive protein (CRP) levels.
undifferentiated SAIDPatients with clinical manifestations consistent with a SAID, after excluding defined monogenic or multifactorial/complex autoinflammatory diseases based on clinical and/or genetic findings. Physician Global Assessment (PGA) > 2 on a 0-10 visual analogue scale (VAS) and elevated C-reactive protein (CRP) levels.
FibromyalgiaWidespread pain with symptoms persisting for at least 3 months. Patients meeting the clinical criteria defined in Wolfe et al. (2016).

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assessment of the usability and usefulness of the SHE system

    The validation should include ≥100 clinical cases and ≥20 end users/evaluators, with a user satisfaction rate of ≥80%, a proportion of correctly classified cases of ≥25%, and an estimated time saved or gained of ≥2 weeks

    Measured: Up to October 2025

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Oct 2026
  2. Study start12 Mar 2025
  3. Primary completion31 Oct 2025
  4. Study completion31 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
73 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07889960
Sponsor's protocol ID
SHE (14101)
Acronym
SHE
Status last verified
Oct 2026
First submitted
12 Oct 2026
Last updated
22 Oct 2026
Results posted
No
FDA-regulated drug
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Systemic Autoinflammatory Diseases (SAID) and Fibromyalgia, run by Istituto Giannina Gaslini at 3 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of the usability and usefulness of the SHE system (time frame: Up to October 2025). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Oct 2026.

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