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Determination of minimum and non-provoking doses of soy protein in soy allergic individuals

Determination of minimum and non-provoking doses of soy protein in soy allergic individuals - Determination of minimum and non provoking doses of soy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON39595
Enrollment
10
Registered
2013-08-19
Start date
2014-01-28
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

food allergy soy allergy

Interventions

None listed

Sponsors

FARRP; Food Allergy Research and Resource Program, Department of Food Science & Technology, University of Nebraska
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Convincing clinical history of a Type I allergic reaction caused by eating soybeans or soy flour 2) Positive skin prick test to the extract of soy flour used to make the oral challenges AND positive specific immunoglobulin E (IgE) to soy (CAP-RAST, Pharmacia Uppsala, Sweden). Subjects should also be skin prick tested with a commercial soy extract. 3) Adults (18-70 years)

Exclusion criteria

Exclusion criteria: 1) Subjects with allergy to wheat 2) Pregnancy

Design outcomes

Primary

MeasureTime frame
To determine minimum and non-provoking doses of soy protein (in mg) for soy allergic individuals.

Secondary

MeasureTime frame
To determine the relevant allergens of soy in soy allergy and to determine the relation between allergen recognition pattern and severity of the allergy.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)