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Examination of pain relief effect of Goreisan for glossodynia

Examination of pain relief effect of Goreisan for glossodynia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs071200017
Enrollment
90
Registered
2020-06-23
Start date
2020-10-30
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 treatment

Sponsors

Ayuse Takao
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. For patients undergoing treatment for glossodynia 2. Age: Adult patients aged over 20 years of age at the time of consent acquisition 3. Gender: Any question 4. hospitalization / outpatient: outpatient only 5. Patients who received written consent by their own free will after thorough understanding before participating in this study

Exclusion criteria

Exclusion criteria: 1.Patients taking Kampo medicines including Goreisan 2.Severe hypertension patients with diastolic blood pressure of 120mmHg or more 3.Patients with severe liver and renal dysfunction 4.Patients with drug hypersensitivity such as allergy 5.Pregnant women and patients who may be pregnant or lactating 6.Patients who participated in another clinical study within 4 months 7.Other patients that the investigator judged to be inappropriate as the study subject

Design outcomes

Primary

MeasureTime frame
Self-filled pain scale (VAS) (Evaluation 12 weeks after administration is the main evaluation point.)

Secondary

MeasureTime frame
1. VAS 2.Salivary amylase activity 3 Tongue examination (whether the veins in the back of the tongue are inflated) 4. Relation to weather information (pressure) (Evaluation 4 weeks and 8 weeks after administration is the main evaluation point.)

Contacts

Public ContactTakao Ayuse

Nagasaki University Hospital

ayuse@nagasaki-u.ac.jp+81-958197713

Outcome results

None listed

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