Rhinosinusitis. Chronic sinusitis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: xylitol nasal spray intervention group is given two puffs every 8 hours for 30 days. Intervention 2: Control group: The second group, or placebo, received normal sa
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with chronic rhinosinusitis Age over 18 years They had previously undergone sinus endoscopy and now need only non-surgical treatments.
Exclusion criteria
Exclusion criteria: Patients who have a history of allergic rhinitis, asthma, immunodeficiency, cystic fibrosis, primary pulmonary dyskinesia, active bacterial or fungal infection and need antibiotics or antifungals Patients who are unsatisfied with non-surgical treatment or want to have surgery again for any reason Have a history of head and neck radiation therapy Now be a smoker Pregnant people Have granulomatous disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lund Kennedy Score. Timepoint: Before and after the study. Method of measurement: Lund Kennedy questionnaire.;SNOT 22 (Sino-nasal Outcome Test) score. Timepoint: Before the intervention and 30 days after the intervention. Method of measurement: SNOT 22 (Sino-nasal Outcome Test).;Severe pain when pressing on the sinuses. Timepoint: Before and after the study. Method of measurement: VAS (Visual Analog Scale) questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAhmad Rezaeian
Esfahan University of Medical Sciences
Outcome results
None listed