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Comparison of aqueous and aerosol beclomethasone sprays in nasal polyps

Phase 3
Recruiting
Conditions
Inflammatory nasal polyp.
Nasal polyp, unspecified
J33.9
Registration Number
IRCT20171030037093N32
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Patients from the age of 18-55 years who suffer from inflammatory nasal polyps
Obtaining written consent to participate in the study

Exclusion Criteria

Previous sensitivity to beclomethasone
Pregnancy or breast-feeding
Severe kidney, heart, liver, neurologic, collagen-vascular, malignancy disease, untreated bacterial or fungal infection
History of trauma and facial fractures
Use of systemic or topical steroids 30 days before study, nasal decongestant, antihistamines, sodium cromolyn, anticholinergics for 7 previous days, use of cardiovascular drugs, neuroleptics, hormones or any drug that causes allergic rhinitis
Tobacco consumption

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The sino-nasal outcomes test-22 average score. Timepoint: Before intervention and 2 months after intervention. Method of measurement: The sino-nasal outcomes test-22 questionnaire.;Lund-Mackay average score. Timepoint: 2 months after intervention (one time). Method of measurement: Sinus CT scan.
Secondary Outcome Measures
NameTimeMethod
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