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Observational study of clinical features of the oral discomfort syndrome

Observational study of clinical features of the oral discomfort syndrome - Oral discomfort syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000024730
Enrollment
100
Registered
2016-11-08
Start date
2016-11-08
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

Oral discomfort syndrome

Interventions

None listed

Sponsors

Tokyo Medical and Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who consulted the psychiatry clinic for symptoms of oral discomfort syndrome. For the purpose of comparison, patients with other psychiatric diagnosis but without oral discomfort syndrome who underwent blood, imaging or psychological tests.

Exclusion criteria

Exclusion criteria: Patiens who declare that the information in their medical records are not to be used for the sutudy.

Design outcomes

Primary

MeasureTime frame
Clinical features of patients with oral discomfort syndrome. Associations between clinical features of oral discomfort syndrome and results of blood, imaging and psychological tests. Associations between drug profiles and treatment response. Differences in results of blood, imaging and psychological tests between patients with and without oral discomfort syndrome.

Countries

Japan

Contacts

Public ContactAkihito Uezato

Graduate School of Tokyo Medical and Dental University Department of Psychiatry and Behavioral Sciences

uezato-tmd@umin.ac.jp03-5803-5242

Outcome results

None listed

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