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Study of the prevalence of aspirin sensitivity in patients with chronic rhinosinusitis and nasal polyposis coming to allergy department of Rasool-e-Akram hospital according to response to standard treatment after three months.

Study of the prevalence of aspirin sensitivity in patients with chronic rhinosinusitis and nasal polyposis coming to allergy department of Rasool-e-Akram hospital according to response to standard treatment after three months.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015061322531N1
Enrollment
100
Registered
2015-07-22
Start date
2015-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

chronic rhinosinusitis with nasal polyposis. Other polyp of sinus Polyp of sinus: accessory ethmoidal maxillary sphenoidal

Interventions

one intervention group which includes conventional treatment for chronic rhinosinusitis with nasal polyposis including intranasal beclomethasone one puff in each nostril twice per day, nasal saline ri
Treatment - Drugs

Sponsors

Vce chancellor for research of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18-65 years old; presence of symptoms of chronic rhinosinusitis with nasal polyps which is documented on CT scan. Exclusion criteria: existence of any serious underlying disease such as bleedin tendency, gastrointestinal, rheumatologic, malignancy, cardiac, renal, hepatic, psychological; history of IgE mediated reactions to aspirin or nonsteroidal anti inflammatory drugs; first second expiratory volume of more than 70 percent of predicted before aspirin challenge test; pregnancy; breast feeding; use of topical and systemic beta blockers; use of warfarin and warfarin derivates; mastocytosis; patients with poor cooperation and poor adherence.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of symptoms of chronic rhinosinusitis with nasal polyposis. Timepoint: after 3 months. Method of measurement: Sino Nasal Outcome Test (SNOT) questionnaire.

Secondary

MeasureTime frame
Complications of conventional treatment including epistaxis, nasal burning sensation, nasal septal perforation, feeling sleepy. Timepoint: before intervention, three months after intervention. Method of measurement: history taking.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSima Shokri

Iran University of Medical Sciences

dr.shokri.83@gmail.com+98 21 6435 2383

Outcome results

None listed

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