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Descriptive Study of Variations in Serum Translocation Markers of the Intestinal Microbiota in Patients With Gougerot-Sjögren Syndrome According to Disease Activity

Descriptive Study of Variations in Serum Translocation Markers of the Intestinal Microbiota in Patients With Gougerot-Sjögren Syndrome According to Disease Activity

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04462601
Acronym
IMISS
Enrollment
50
Registered
2020-07-08
Start date
2020-11-13
Completion date
2028-10-31
Last updated
2025-11-17

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

Conditions

Sjogren's Syndrome

Brief summary

Gougerot-Sjögren syndrome or Sjögren syndrome is a chronic autoimmune disease belonging to connectivitis, the classic triad of symptoms being the association of a sicca syndrome (generally predominant in the mouth and / or ocular, but also present at the cutaneous, vaginal or tracheal level), diffuse arthromyalgia and marked fatigue. The study investigators hypothesize that changes in the gut microbiota, by modulating gut permeability and thereby promoting microbial translocation, would have immunomodulatory effects that could be correlated to changes in the activity of Gougerot-Sjögren disease.

Interventions

Quantification of serum markers of intestinal permeability and bacterial and fungal translocation

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The patient must be a member or beneficiary of a health insurance plan * Patients with primary Sjögren's syndrome according to the AECG criteria

Exclusion criteria

* The subject is participating in a category I interventional study, or is in a period of exclusion determined by a previous study * It is impossible to give the subject informed information * The patient is under safeguard of justice or state guardianship * Pregnant, parturient or breastfeeding patients * Patients with secondary Sjögren's syndrome

Design outcomes

Primary

MeasureTime frameDescription
Difference in Intestinal Fatty Acid Binding Protein (I-FABP) levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)ng/ml measured by ELISA; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)
Difference in zonulin-1 levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)ng/ml measured by ELISA; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)

Secondary

MeasureTime frameDescription
Difference in LPS-binding Protein levels between patients receiving or not systemic treatment (corticosteroids, plaquenil or methotrexate)Upon changing disease activity level (maximum 3 years)pg/ml, measured by ELISA
Difference in soluble CD14 levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)ng/ml, measured by ELISA; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)
Difference in soluble CD14 levels from baseline in patients reporting an improvement in disease activityUpon changing disease activity level (maximum 3 years)ng/ml, measured by ELISA; patient-reported disease severity defined by 1-point increase on the European League Against Rheumatism Sjögren's syndrome Patient Reported Index (ESSPRI)
Difference in soluble CD14 levels between patients receiving or not systemic treatment (corticosteroids, plaquenil or methotrexate)Upon changing disease activity level (maximum 3 years)ng/ml, measured by ELISA
Difference in fungal 18s RNA levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)PCR and sequencing; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)
Difference in fungal 18s RNA levels from baseline in patients reporting an improvement in disease activityUpon changing disease activity level (maximum 3 years)PCR and sequencing; patient-reported disease severity defined by 1-point increase on the European League Against Rheumatism Sjögren's syndrome Patient Reported Index (ESSPRI)
Difference in fungal 18s RNA levels between patients receiving or not systemic treatment (corticosteroids, plaquenil or methotrexate)Upon changing disease activity level (maximum 3 years)PCR and sequencing
Difference in LPS-binding Protein levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)pg/ml, measured by ELISA; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)
Difference in bacterial 16s RNA levels from baseline in patients reporting an improvement in disease activityUpon changing disease activity level (maximum 3 years)PCR and sequencing; patient-reported disease severity defined by 1-point increase on the European League Against Rheumatism Sjögren's syndrome Patient Reported Index (ESSPRI)
Difference in bacterial 16s RNA levels between patients receiving or not systemic treatment (corticosteroids, plaquenil or methotrexate)Upon changing disease activity level (maximum 3 years)PCR and sequencing
EQ-5D-5L questionnaireBaselinescore 0-100
World Health Organization Quality Of Life BREF questionnaireBaselinescore 0-100
Hospital Anxiety and Depression ScaleBaselinescore 0-42
Multidimensional Fatigue InventoryBaselinescore 4-20
Difference in bacterial 16s RNA levels from baseline in patients passing to a different level of disease activityUpon changing disease activity level (maximum 3 years)PCR and sequencing; Change in disease activity levels defined by 3-point change on the European League Against Rheumatism Sjögren Syndrome Disease Activity Index (ESSDAI)
Difference in LPS-binding Protein levels from baseline in patients reporting an improvement in disease activityUpon changing disease activity level (maximum 3 years)pg/ml, measured by ELISA; patient-reported disease severity defined by 1-point increase on the European League Against Rheumatism Sjögren's syndrome Patient Reported Index (ESSPRI)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026