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Surveys of patients with Sjogren's syndrome prior to diagnosis and at the present in Japan

Surveys of patients with Sjogren's syndrome prior to diagnosis and at the present in Japan - Surveys in Sjogren's syndrome in Japan

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000037531
Enrollment
800
Registered
2019-10-01
Start date
2019-10-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Sjogren&#39

Interventions

None listed

Sponsors

Kochi University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Paients with Sjogren's sydrome and Members in the Japanese Sjogren's association for patients (JSAP)

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
period from when a patients noticed unusual symptoms to when Sjogren syndrome was diagnozed.

Secondary

MeasureTime frame
details of the symptoms, how a patient was diagnozed by and how many hospitals a patients had visted until the diagnosis

Countries

Japan

Contacts

Public ContactKaori Komori

Kochi Medical School Department of Enviromental Medicine

jm-kaorikomori@kochi-u.ac.jp+81888802407

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026