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Effect of Extract of Urtica dioica on perennial Allergic Rhinitis

Effect of Extract of Urtica dioica on perennial Allergic Rhinitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013102715177N1
Enrollment
20
Registered
2013-11-19
Start date
2013-05-10
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

Allergic Rhinitis. Other allergic rhinitis

Interventions

Intervention 1: Intervention group: The patients were treated with urtica dioica (150 mg qid for one month. Intervention 2: Control group:The patients were treated with placebo for one month.
Treatment - Drugs
Placebo
Intervention group: The patients were treated with urtica dioica (150 mg qid for one month
Control group:The patients were treated with placebo for one month.

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Clinical and laboratory diagnosis perennial allergic rhinitis; Patients' willingness to participate in treatment and plan Exclusion criteria: The risk of other causes of rhinitis; Systemic diseases such as polycythemia; Use of other drugs with anti-inflammatory properties;Use of any herbal remedy; Intolerance of side effects urtica dioica; Drug use weak immune system; Use of antidiabetic drugs; Use of hypertensive drugs; Pregnancy & Breastfeeding; Age less than 15 years and more than 45 years.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Symptoms of Allergic rhinitis. Timepoint: Befor and after treatment. Method of measurement: SNOT - 22.

Secondary

MeasureTime frame
Blood level of IgE. Timepoint: Before and after treatment. Method of measurement: ELISA.;Blood level of IL5. Timepoint: Before and after treatment. Method of measurement: ELISA.;Blood level of IL4. Timepoint: Before and after treatment. Method of measurement: ELISA.;Blood level of INF Gamma. Timepoint: Before and after treatment. Method of measurement: ELISA.;Nasal eosinophil count. Timepoint: Before and after treatment. Method of measurement: Eosinophil count.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Bakhshaee

Mashhad university of Medical Science

Bakhshaeem@mums.ac.ir+98 51 1859 4082

Outcome results

None listed

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