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Ultrafast immunotherapy in allergic rhinitis

Evaluate clinical and immunological efficacy of subcutaneous allergen immunotherapy with three-day rush immunotherapy or ultra-rush immunotherapy method in allergic rhinitis for the first time in Iran

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010123235N8
Enrollment
21
Registered
2017-06-25
Start date
2015-05-22
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. Perennial allergic rhinitis

Interventions

Intervention involving consumption of allergen condensed Extract including saline grass and combination of weeds bought from GREER company for immunotherapy, Intervention involving consumption of
Treatment - Drugs

Sponsors

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

Eligibility

Sex/Gender
All
Age
15 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The risk of perennial allergic rhinitis; Positive skin test to allergens in the air; Clinical signs associated with skin test Exclusion criteria: History of autoimmune disease; Patients with systemic corticosteroids or immunosuppressive drugs for reasons other than allergic disease on the immune system use to be effective; Pregnancy; Immunocompromised patients, patients who have uncontrolled allergic asthma; Patients with malnutrition; Patients who received beta-blocker drugs; Patients with a history of anaphylaxis; patients With coexisting cardiovascular disease; During treatment, patients who are experiencing systemic reactions; Patients with mental disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical symptoms. Timepoint: Befor the trial. Method of measurement: questionnaire.

Secondary

MeasureTime frame
FOXP3. Timepoint: 3 month later. Method of measurement: Flowcytometry.;IFN-?. Timepoint: 3 month later. Method of measurement: Flowcytometry.;IL-4. Timepoint: 3 month later. Method of measurement: Flowcytometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Fouladvand

Mashad Universityof Medcal Sciences

Dr.fooladvand@yahoo.com+98 51 3801 2830

Outcome results

None listed

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