MedPath

Effect of Xylitol nasal spray in treatment of chronic rhinosinusitis

Phase 2
Conditions
Rhinosinusitis.
Chronic sinusitis, unspecified
J32.9
Registration Number
IRCT20171030037093N35
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
und 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.
Secondary Outcome Measures
NameTimeMethod
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