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Evaluation of the therapeutic effect of fluconazol drop on chronic rhinosinusitis

Evaluation of the therapeutic effect of fluconazol drop on chronic rhinosinusitis in patients reffered to otorhinolarnyngology clinic in Hamadan

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138811063186N1
Enrollment
54
Registered
2011-08-02
Start date
2009-04-04
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

rhinosinusitis. Bacterial, viral and other infectious agents

Interventions

Intervention 1: Intervention group: drop bottles including fluconazole 2%. is used 2 times per day (4 drops) for 2 months, also beclomethasone nasal spray is used 2 times per day (2 puffs) for 2 month
Treatment - Drugs
Placebo
Intervention group: drop bottles including fluconazole 2%. is used 2 times per day (4 drops) for 2 months, also beclomethasone nasal spray is used 2 times per day (2 puffs) for 2 months.
Control group: drop bottles with the appearance identical to intervention group, includes normal saline which is used 2 times per day, 4 drops, for 2 months. Also beclomethasone nasal spray is used 2

Sponsors

Hamedan University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: the patients with diagnosis of chronic rhinosinusitis according to American Academy of Otolaryngology which have no response to medical therapy; Exclusion criteria: known sensitivity to fluconazole; pregnancy and breast feeding women; immune compromised patients; patients with acute complication of CRS; superimposition of ARS(fever, acute pain, pressure on face); antibiotic use in recent 7 days ; age below 18 years; systemic antifungal use in recent 7 days and systemic steroid use in recent 30 days

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Snot-20. Timepoint: 2 months. Method of measurement: Check list.;CT score. Timepoint: 2 months. Method of measurement: Check list.

Secondary

MeasureTime frame
Side effect. Timepoint: 2 months. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnaz Hashemian

Hamedan University of Medical Science

hashemianf@yahoo.com; hashemian@umsha.ac.ir+98 81 1264 0039

Outcome results

None listed

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