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Wheat oral desensitization in patient with wheat allergy

Evaluation of efficacy and safety of wheat oral immunotherapy in patient with wheat allergy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204199510N1
Enrollment
15
Registered
2014-02-26
Start date
2012-06-21
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

Condition 1: wheat allergy. Condition 2: Desensitization. Adverse effects, not elsewhere classified Desensitization to allergens

Interventions

The anaphylactic patients take Loratadine and Montelukast, three days prior to admission to prevent the severe adverse reaction. On the first day of admission
we perform OFC again with premedication, so we determine the initial dose of rush OIT. In rush phase, patients take bread two time a day, and if they can take them without severe reactions, they are
Treatment - Other

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients above 5 years with IgE mediated wheat allergy (positive skin prick test response to wheat flour and wheat specific IgE level above 0.35 IU/L); positive oral food challenge to wheat. exclusion criteria: severe and uncontrolled asthma; chronic urticaria; significant systemic disease; poor compliance

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Daily consumption of wheat products without any complications. Timepoint: Before oral immunotherapy and 3 month after starting maintenance phase. Method of measurement: Oral food challenge with 52 gr of bread containing 5.2 g wheat protein.

Secondary

MeasureTime frame
Evaluation of skin, respiratory, gastrointestinal symptoms and anaphylaxis reaction during course of treatment. Timepoint: During buildup and maintenance phase. Method of measurement: Number of participants with adverse events and observation of their sign and symptoms.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Khayatzadeh

Department of Allergy and Clinical Immunology in Children's Medical Center at Tehran University of M

a-khayatzadeh@razi.tums.ac.ir+98 21 6147 2153

Outcome results

None listed

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