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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03681964
Other study ID # DIApSS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 28, 2015
Est. completion date September 28, 2030

Study information

Verified date July 2018
Source University Hospital, Brest
Contact Valerie Devauchelle, MD,PhD
Phone 33 (0) 2 98 34 72 64
Email valerie.devauchelle-pensec@chu-brest.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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)


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 28, 2030
Est. primary completion date September 28, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with suspected pSS underwent a standardised evaluation

Exclusion Criteria:

- Opposition of patient

Study Design


Locations

Country Name City State
France CHRU de Brest Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary classification criteria classification criteria at inclusion of patients with suspected primary Sjögren's syndrome (pSS) underwent with standardised evaluation Inclusion (Day 0)
See also
  Status Clinical Trial Phase
Completed NCT05269810 - Clinical Study to Investigate the Efficacy of Orally Administered SA001 in Patients With Primary Sjögren's Syndrome Phase 2
Completed NCT01782235 - Efficacy of Tocilizumab in Primary Sjögren's Syndrome. Phase 2/Phase 3
Recruiting NCT05113004 - New Clinical End-points in Patients With Primary Sjögren's Syndrome Phase 2