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Effect of local injection of botulinum toxin versus nasal fluticasone spray on clinical sign and symptoms in patients with allergic rhinitis

Phase 2
Conditions
Allergic rhinitis.
Allergic rhinitis, unspecified
Registration Number
IRCT201506079014N67
Lead Sponsor
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
74
Inclusion Criteria

(a) age of 18 to 70 years; (b) having allergic rhinitis.
Exclusion criteria: (a) pregnancy or breastfeeding; (b) contraindication of corticosteroids; (c) having severe anatomical abnormality in nose or acute rinosinusitis; (d) having glaucoma or prostatic hypertrophy; (e) having severe systemic diseases such as diabetes or asthma; (f) simultaneous using aminoglycoside drugs.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessing nasal congestion. Timepoint: 8 weeks after intervention. Method of measurement: through physical examination.;Assessing rhinorrhea. Timepoint: 8 weeks after intervention. Method of measurement: through taking history.;Assessing nasal itching. Timepoint: 8 weeks after intervention. Method of measurement: through taking history.;Assessing sneezing. Timepoint: 8 weeks after intervention. Method of measurement: through taking history.
Secondary Outcome Measures
NameTimeMethod
Assessing dizziness. Timepoint: 8 weeks after intervention. Method of measurement: through taking history.
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