Examination of the pain relief effect of Goreisan for glossodynia with dry mouth 2

Examination of the pain relief effect of Goreisan for glossodynia with dry mouth 2 - Examination of the pain relief effect of Goreisan for glossodynia 2

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037705

Enrollment

Registered

2019-08-16

Start date

2019-09-01

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

Glossodynia

Interventions

Goreisan

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patients who have been diagnosed with glossodynia with dry mouth and are undergoing treatment at the oral pain liaison outpatient department of Nagasaki University Hospital 2)Age: Adult patients older than 20 years old when obtaining consent 3)Gender: Any 4) Hospitalization / Outpatient: Outpatient only 5)Patients who have received sufficient explanation for participation in this study, and who have received sufficient written consent from the patient himself / herself with sufficient understanding

Exclusion criteria

Exclusion criteria: 1) Patients taking Chinese medicine other than Gojosan 2)Patients with severe hypertension whose diastolic blood pressure is 120mmHg or more 3) Patients with severe liver and renal dysfunction 4) Patients with allergies and other drug sensitivity 5) Pregnant women and patients who may be pregnant or breastfeeding 6) Other patients who are deemed inappropriate by the research director

Design outcomes

Primary

Measure	Time frame
Self-filled pain scale (VAS)	—

Countries

Japan

Contacts

Public ContactTAKAO AYUSE

Nagasaki University Hospital Deantal Anesthesia

ayuse@nagasaki-u.ac.jp0958197713

Outcome results

None listed

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