ICU patients
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Adult patients who have given written consent to participate in the study 2)Patients scheduled to be admitted to the ICU or admitted as an emergency 3)The period of prohibited eating and drinking is longer than 24 hours. 4)GCS:E3V5(T)M6, sedation depth at RASS 0. Patients who can communicate. 5)Patients who do not have ulcers in their mouths or who do not have the potential for pain. 6)Patients who do not have a problem with menthol
Exclusion criteria
Exclusion criteria: 1)Blood sodium concentration is 150 mEq/L or more 2)Patients who have difficulty communicating in Japanese and reading and writing in Japanese 3)Patients whose inclusion in the study is deemed inappropriate by the investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Subjective Thirst Analog Scale Immediately After Oral Care Implementation | — |
Secondary
| Measure | Time frame |
|---|---|
| The number of hours of oral care the patient wanted after implementation | — |
Countries
Japan
Contacts
Center Hospital of the National Center for Global Health and Medicine Nursing department