Thirst
Conditions
Interventions
Allocation groups
All groups were instructed by the researcher to fast for a period of 8 hours, and no liquids or solids should be ingested.
Control Group (N=20)
The volunteer allocated to the contro
Sponsors
Universidade Estadual de Londrina
Universidade Estadual de Londrina
Eligibility
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Be aged between 18 and 50 years old be of both sexes. Be fasting for 8 hours of solids and liquids
Exclusion criteria
Exclusion criteria: Being allergic to menthol Being allergic to one of the components of the product Present nausea or vomiting during the approach Present salivary dysfunctions Present lesions or dysfunctions in the oral cavity Having the flu or having a respiratory condition being a smoker or having chronic diseases such as hypertension and diabetes Present salivary dysfunctions present lesions in the oral cavity brush your teeth at least 2 hours before collection smoker drink alcoholic beverages for 24 hours perform physical exercises for 60 minutes before collection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Thirst intensity: variation of the initial thirst intensity in relation to the final one presented by the experimental group (EG), placebo group (PG) and control group (CG). | — |
Secondary
| Measure | Time frame |
|---|---|
| Defining characteristics of the headquarters: presence or absence of defining characteristics of the headquarters by the EG, GP and GC at 15, 30 and 45 minutes after its application.;Hydrogenonic potential (pH): variation of the initial pH in relation to the final one presented by the GE, GP and GC.;Oral mucosa hydration: variation of initial oral mucosa hydration in relation to the final one presented by the EG, GP and CG. | — |
Countries
Brazil
Contacts
Public ContactRobertha;Ligia Juvencio Silva;Fahl Fonseca
Universidade Estadual de Londrina;Universidade Estadual de Londrina
Outcome results
None listed