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Comparison of aqueous and aerosol beclomethasone sprays in nasal polyps

A copmarison of beclomethasone aqueous spray and aerosol delivery system in nasal polyps: A randomized control trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171030037093N32
Enrollment
70
Registered
2020-03-14
Start date
2020-02-22
Completion date
Unknown
Last updated
2020-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory nasal polyp. Nasal polyp, unspecified

Interventions

Intervention 1: First intervention group: Patients in the first group are treated with beclomethasone nasal spray produced by Raha pharmaceutical company 50 µg/dose 2 puff in each nose per day for 2 m

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Rezaeian

Esfahan University of Medical Sciences

ahmadrezaeian@med.mui.ac.ir+98 31 3445 2031

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026