Significance of an Elimination and Provocation Diet in Patients With Chronic Urticaria
Information source: University Hospital Muenster
Information obtained from ClinicalTrials.gov on December 31, 2007 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Urticaria; Angioedema
Intervention: elimination diet (Procedure); provocation diet (Procedure)
Phase: N/A
Status: Active, not recruiting
Sponsored by: University Hospital Muenster Official(s) and/or principal investigator(s): Randolf Brehler, senior MD, Principal Investigator, Affiliation: University Hospital Münster, Department of Dermatology
Summary
Patients with chronic urticaria undertake a five week elimination diet (pseudoallergen free
diet). The efficacy of the diet will be determined by symptom score, by the use of rescue
medication (oral antihistamines and glucocorticosteroids) and by a Quality of Life
Questionnaire on week 0 and week 5. All patients with sufficient response (regarding the
urticaria score) enter a second dietary part over six weeks, whereas a provocation diet is
carried out. Each diet week a choice of pseudoallergen rich food is added, sorted by the type
of pseudoallergens (e. g. biogenic amines, organic acids, flavours, additives). This study is
conducted to investigate if the provocation diet could be a new diagnostic intervention to
elucidate clinical relevant pseudoallergens.
Clinical Details
Official title: Significance of an Elimination and Provocation Diet in Patients With Chronic Urticaria
Study design: Screening, Cross-Sectional, Defined Population, Prospective Study
Detailed description:
Chronic urticaria is defined as a daily or almost daily spontaneous occurrence of wheals that
cause itching and lasting for at least six weeks. If there is no indication of a possible
eliciting agent and because approximately 70% of patients benefit from it, a
low-pseudoallergen diet should be carried out for 5 weeks. Although the low-pseudoallergen
diet is successful, no explanation of the underlying mechanisms exists. On DBPC oral
provocation testing with known food additives, only a small amount of patients, who
experienced remission after a low-pseudoallergen diet react with new wheals and/or
angioedema. For this discrepancy, natural food ingredients and new food additives are
included in the dietary diagnostic. The high amount of substances, which are administrated
within oral provocation testing can not reflect a realistic diet situation. Often it is
impossible to ingest corresponding amounts of foods to reach the same concentration such as
the provocation amount. Recording change reactions between food ingredients and the
individual metabolism of the patients, the "step by step" food provocation method reveals
itself to be most effective. In addition, individual predilections, amounts and frequency of
ingested foods, are taken into consideration.
Eligibility
Minimum age: 7 Years.
Maximum age: 80 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
signed informed consent
chronic urticaria (duration: at least 6 weeks)
patients who suffered from urticaria and/or angio oedema at least once a week for a
duration of at least 4 weeks)
Males and females, age between 7 and 80 years
inpatients and outpatients
oral antihistamines and glucocorticosteroids are allowed as concomitant medication (if
needed)
Exclusion Criteria:
pregnant or breastfeeding woman
patients suffering from diabetes mellitus
patients with cachexia
known food allergies of food which will be administrated within the elimination diet (e. g.
milk, cereals)
isolated urticaria with known aetiology (e. g. physical urticaria, aquagene urticaria,
urticaria factitia, cholinergic urticaria), Urticaria pigmentosa mastocytoses)
patients, seemed to be uncompliant under suspicion of the investigator
Locations and Contacts
University Clinics of Münster, Department of Dermatology, Münster 48149, Germany
Additional Information
Starting date: January 2005
Ending date: April 2007
Last updated: February 26, 2007
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