Recruiting NCT03681964
Diagnostic Suspicion of Primitive Syndrome Sjögren's : Brest Cohort
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Primary Sjögren's Syndrome (pSS). Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This study aims to evaluate the diagnosis performance of several item used for the classification, the diagnosis and the prognostic of pSS (primary Sjogren syndrome)
Primary outcome measures
- classification criteria [Time frame: Inclusion (Day 0)]
Eligibility criteria
Inclusion criteria
- Patients with suspected pSS underwent a standardised evaluation
Exclusion criteria
- Opposition of patient
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- CHRU de Brest — Brest
Identifiers
NCT: NCT03681964 · DIApSS