Chemotherapy-and/or radiation-induced oral mucositis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy male adult Body weight over 50 kg BMI over 18.5 under 25.0 kg/m2 Subjects without dysgeusia Nonsmokers Having given written informed consent prior to any procedure related to the study
Exclusion criteria
Exclusion criteria: Subjects using medical products Subjects who could start having allergic symptom in relation to test products Subjects with a disease of the oral mucous membrane (including a wound in the mouth) or subjects under dental treatment Subjects judged inappropriate for the study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of threshold of saltiness by test paper (SALSAVE) | — |
Countries
Japan
Contacts
Pharmaspur Inc. Clinical study