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Investigating the effect of glucosamine in allergic rhinitis

Investigating the effect of glucosamine in patients with allergic rhinitis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200411047021N2
Enrollment
80
Registered
2024-09-29
Start date
2024-02-08
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Allergic rhinitis. Allergic rhinitis, unspecified

Interventions

Intervention 1: Control group: patients with allergic rhinitis treated with placebo tablets once a day (similar to glucosamine tablets but containing sugar) manufactured by Abidi Pharmaceuticals for 1

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with allergic rhinitis Diagnosis of allergic rhinitis by an otolaryngologist Allergic rhinitis more than 12 weeks ?? ????? 18 ??? ??? ???? ?? ????? ??? ????? (???? ???????? ? ????? ??? ?????)

Exclusion criteria

Exclusion criteria: Hypersensitivity to glucosamine or similar compounds The presence of hypersensitivity reactions in the patient Existence of systemic diseases (such as diabetes, hypertension, dyslipidemia, etc.) Patients who have tumors in the nose and sinuses Patients who have had any surgery on the nose and sinuses.

Design outcomes

Primary

MeasureTime frame
Serum IgE level. Timepoint: before and after the 15 days course of treatment. Method of measurement: blood sample.;Total nasal symptom scores. Timepoint: before and after the 15 days course of treatment. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Rezaeian

Esfahan University of Medical Sciences

dr.ahmadrezaeian@gmail.com+98 31 3265 1574

Outcome results

None listed

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