Inclusion criteria | Exclusion criteria |
---|---|
Confirmed allergic rhinitis | Mental disorders |
Sensitive to Artemisia pollen allergens | Systemic disease that the researchers consider to interfere with the study |
Aged 18–65 years | Aged under 18 years or over 65 years |
Provided informed consent and volunteered to participate in this clinical trial | Not cooperative during examination |
Completed the case report form and other records | Employment changes leading to a possible loss to follow-up |
Dysgnosia or behavioral disorders | |
The following conditions: nasal polyps, chronic sinusitis, severe nasal deviation, rhinitis medicamentosa, primary sleep disorders (> 1 night/week), obstructive sleep apnea, upper respiratory infection within 2 weeks prior to enrollment, or poorly controlled asthma | |
Pregnant or may become pregnant, or lactating with a positive urine pregnancy test | |
Drug abuse within the past 3 years | |
Must sleep in different bed more than six times in 3 weeks or for more than 3 consecutive nights | |
Smoked within the past 1 year | |
Sensitive to indoor allergens such as dust mites and pet dander | |
Other reasons, at the investigator’s discretion | |
Refusal to continue the trial because of a poor curative effect | |
Refusal to continue the trial for an unspecified reason | |
Loss to follow-up because of a change of address or telephone number | |
Loss to follow-up because of personal reasons |