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Clinical Trial Summary

The objectif is to study the diagnosis performance of the different classification criteria in reference to the gold standard consisting of the diagnosis made by expert doctors after standardized assessment, of pSS (primary Sjogren syndrome)


Clinical Trial Description

The formation of this patient is single-center prospective intervention. It consists of collecting data from patients suspected of pSS from standardized biological clinical data and imaging examination and additional pathology. - Sjögren patients will be followed at inclusion, 2y, 3y, 4y, 6y, 8y and 10 years. Blood, fluid, sells and urine samples will be collected at inclusion, 4y et 10y. - Non-Sjögren controls will be followed at inclusion and 4y and samples will be collected at the same visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04931160
Study type Interventional
Source University Hospital, Brest
Contact Valérie Devauchelle, MD,PhD
Phone 33 (0) 2 98 34 72 64
Email valerie.devauchelle-pensec@chu-brest.fr
Status Recruiting
Phase N/A
Start date February 10, 2020
Completion date February 10, 2035

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