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The non-blind test crossover controlled trial how we used a physically unimpaired person volunteer about quantity of salivary secretion increase action of gargle remedy of cevimeline hydrochloride hydrate

The non-blind test crossover controlled trial how we used a physically unimpaired person volunteer about quantity of salivary secretion increase action of gargle remedy of cevimeline hydrochloride hydrate - A controlled trial about quantity of salivary secretion increase action of gargle remedy of cevimeline hydrochloride hydrate

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000000997
Enrollment
12
Registered
2008-01-28
Start date
2008-01-01
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

Xerostomia due to Sjogren`s syndrome

Interventions

It is a gargle with a test drug(Cevimeline hydrochloride hydrate 30mg+Hachiazule(TM)gargle 2g+distilled water 50cc)for two minutes. wash out, It is a gargle with false placebo1 (Cevimeline hydrochlor

Sponsors

Department of Dentistry and Oral Surgery, Tochigi National Hospital
Lead Sponsor
National Institute of Public Health
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A gum test value is 10ml/10min excess. The person who does not have a feeling of xerostomia. The person who gets mutual understanding.

Exclusion criteria

Exclusion criteria: The person that a gargle is impossible. A person we have a history of sick treatment of facial nerve or is treating the present. A person we have a history of sick treatment of trigeminus or is treating the present. A person we have a history of salivary gland conditions treatment within six months before this agent administration start or is treating the present. A person of diabetes mellitus. A person having an extensive oral mucosa disorder. The person who took the medicine that it was thought that we had an influence on salivary secretion during taking again within examination one month. It is a hypersensitivity symptom and a person having contraindication in cevimeline hydrochloride hydrate and Hachiazule(TM) gargle. The pregnancy and a woman nursing or a woman with pregnant likelihood. In addition, the person who admitted that we were inappropriate though a study director performed the final examination.

Design outcomes

Primary

MeasureTime frame
It is amount of increase in the unstimulated whole saliva secretion after gargle 90 minutes, gargle 60 minutes later, gargle 30 minutes later and gargle 15 minutes later.

Countries

Japan

Contacts

Public ContactHiroshi Iwabuchi

Tochigi National Hospital Department of Dentistry and Oral Surgery

hiwabuch@tochi.hosp.go.jp028-622-5241

Outcome results

None listed

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