Seasonal allergic rhinitis
Conditions
Interventions
The mouthpiece is set during the onset of allergic rhinitis symptoms (sneezing, runny nose, stuffy nose).
Normal subjects who did not develop pollen symptoms were used as a control group.
Sponsors
Department of Oral Integrated Medicine Kanagawa Dental University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Hospitalized patients with symptoms of allergic rhinitis (house dust, PM 2.5 etc) visit our Kanagawa Dental hospital.
Exclusion criteria
Exclusion criteria: 1) Those who are undergoing treatment due to infection with hemophilia, hepatitis, HIV, etc, and who are at risk of treatment due to high blood pressure, diabetes etc. 2) Pregnant women or lactating women 3) Person who has participated in the trial within 12 weeks before the start of this procedure 4) Person who judged that the dental clinic in charge is not appropriate for other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate relief of allergic rhinitis symptoms before and after mouthpiece attachment by allergic rhinitis severity classification. | — |
Secondary
| Measure | Time frame |
|---|---|
| Furthermore, changes in salivary secretion rate, salivary IgA concentration, salivary IL-33 concentration, and saliva properties are evaluated. | — |
Countries
Japan
Contacts
Public ContactNobuyuki Tani-Ishii
Department of Oral Integrated Medicine ,Kanagawa Dental University Division of Pulp Biology
Outcome results
None listed