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Eye Dryness Evaluation in Primary Sjögren's Syndrome

NCT03614299 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2025-02-05

No results posted yet for this study

Summary

The objective of this observational study is to develop new tools to assess primary Sjögren's syndrome (pSS) symptoms and to measure the severity of eye involvement in these patients.

Conditions

  • Primary Sjögren Syndrome

Interventions

OTHER

Ecological symptom measurements using a webapp

A webapp will be installed on the patients' smartphone, which will be used to collect everyday the symptoms of the patients (ESSPRI score)

DIAGNOSTIC_TEST

Interferometry

Evaluation of the mebomian function using the LipiView methodology

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-20
Primary Completion
2020-08-28
Completion
2020-08-28

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03614299 on ClinicalTrials.gov