Allergic Rhinitis. Allergic rhinitis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: receiving herbal nasal spray made by researchers in the pharmaceutical laboratory of the school of Persian and Complementary medicine of Mashhad University of Medic
with the order of 2 puffs every 8 hours inside each nasal cavity for 3 weeks. Intervention 2: Control group: receiving a placebo nasal spray made by researchers in the pharmaceutical laboratory of the
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: All patients 18 years to 70 years old that according to the ARIA guideline and diagnosis of a clinical Immunologist have allergic rhinitis
Exclusion criteria
Exclusion criteria: Diffused Nasal Polyps Pregnancy History of allergy to Coriander or Bitter orange Asthmatic patients Systemic inflammatory diseases Using antihistamines during the last week before the beginning of the study Using inhaled corticosteroids during the last 2 weeks before the beginning of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nasal obstruction. Timepoint: Baseline and 3 weeks after intervention. Method of measurement: Total Nasal Symptom Score questionnaire.;Itching/Sneezing. Timepoint: Baseline and 3 weeks after intervention. Method of measurement: Total Nasal Symptom Score questionnaire.;Rhinorrhea. Timepoint: Baseline and 3 weeks after intervention. Method of measurement: Total Nasal Symptom Score questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Symptom recurrence rate. Timepoint: Baseline and one week after the end of intervention. Method of measurement: Rhinitis Control Assessment Test (RCAT) questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAlieh Farabi
Mashhad University of Medical Sciences
Outcome results
None listed