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clinical trial of the effect of raw and cooked milk immunotherapy in children with milk allergy

Comparison of the effect of oral immunotherapy with cow's milk products and conventional desensitization in children with allergy to heated cow's milk: a clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170426033658N2
Enrollment
25
Registered
2018-04-01
Start date
2016-04-29
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

food allergy. Allergy, unspecified

Interventions

Intervention 1: In the intervention group, certain amount of muffin is given to patients and they are monitored for 4 hours under medical observation. Then desensitization with 1.8 muffin's slice is i

Sponsors

Vice chancellor for Research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 15 Years

Inclusion criteria

Inclusion criteria: patients two years and older Presentation of skin symptoms such as urticaria, erythema and angioedema gastrointestinal symptoms such as severe vomiting, abdominal pain and diarrhea respiratory symptoms such as rhinitis and bronchospasm Presentation of the symptoms up to two hours after exposure these symptoms should be present at least in last six months positive skin prick test for cow's milk or measurement of sIgE for cow's milk positive challenge test with cow's milk

Exclusion criteria

Exclusion criteria: cellular immune response that is not mediated by IgE malignancy or severe immunodeficiency disorders using beta blockers uncontrolled severe persistent asthma Cardiovascular disease that epinephrine administration is contraindicated in them Taking immunosuppressive drugs previously diagnosed Eosinophilic Gastrointestinal Disorder in response to milk

Design outcomes

Primary

MeasureTime frame
Regulatory T cell. Timepoint: Before intervention, after intervention. Method of measurement: Flow cytometry.;Specific IGE for milk. Timepoint: Before intervention, after intervention. Method of measurement: RIDA.;Milk Desensitization. Timepoint: Before intervention, after intervention. Method of measurement: Clinical.

Secondary

MeasureTime frame
Symptoms,anaphylaxis,desensitization. Timepoint: Immediately after intervention. Method of measurement: physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Emad Bahraminiya

Tehran University of Medical Sciences

bahraminiya.emad@gmail.com+98 21 61479

Outcome results

None listed

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