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Sub lingual immunotherapy of Nasal allergies

Evaluation of clinical and immunological efficacy of sub lingual immunotherapy in patients with allergic rhinitis sensitive to mite

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017042323235N9
Enrollment
40
Registered
2017-05-10
Start date
2010-03-20
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

Perennial allergic rhinitis. Other allergic rhinitis

Interventions

Intervention 1: In Intervention group received Extract drops of mite via sublingual administration for 6 months. Intervention 2: In control group received placebo via for 6 months.
Treatment - Drugs
Placebo
In Intervention group received Extract drops of mite via sublingual administration for 6 months
In control group received placebo via for 6 months

Sponsors

Vice chancellor for research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:approved clinical perennial allergic rhinitis and laboratory diagnosis;the desire of patients to drug treatment and participation in the project Exclusion criteria: Suffering from seasonal allergic rhinitis, a history of autoimmune disease, Consumption of corticosteroids or immunosuppressive drugs, pregnancy, allergic asthma, malnutrition

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical symptoms of allergic rhinitis. Timepoint: After six month. Method of measurement: questionnaire.

Secondary

MeasureTime frame
FOXP3 gene expression. Timepoint: After six month. Method of measurement: Real-Time PCR.;Interlukin-10. Timepoint: After six month. Method of measurement: Real-Time PCR.;Tumor Groeth Factor-B. Timepoint: After six month. Method of measurement: Real-Time PCR.;Interlukin-17. Timepoint: After six month. Method of measurement: Real-Time PCR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoma sadri

Mashad Universityof Medcal Sciences

homasadri7@gmail.com+98 518012770

Outcome results

None listed

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