Medical University of Warsaw
Warsaw, 02-091, Poland
NCT Number: NCT05923216
This is an experimental, interventional study, following on from a clinical trial comparing the efficacy and safety of oral immunotherapy with low and high doses of sesame protein, in which patient desensitisation was achieved (High and Low Dose Oral Sesame Immunotherapy - Comparison of Efficacy and Safety, NCT05158413).
The aim of this study is to assess a sustained unresponsiveness (SU) to sesame protein after at least 8 months of previously assigned high- or low-dose sesame OIT, followed by 4-week-allergen avoidance, and verified by an open oral food challenge (OOFC).
Interested in participating?
Request Info4 year–17 year
All sexes
Interventional
Not applicable
Warsaw, 02-091, Poland
Oral immunotherapy is considered the most effective treatment for food allergy. There are two main goals of food immunotherapy: achievement of desensitisation and sustained unresponsiveness.
Desensitisation involves achieving temporary tolerance of the allergenic food by the patient only during regular intake of the allergen. The most desirable effect of immunotherapy is to achieve sustained unresponsiveness, i.e. to maintain the absence of adverse symptoms to a given allergen after specific immunotherapy has been discontinued for a defined period of time.
The study is a continuation of a clinical trial NCT05158413 which was designed to compare the efficacy and safety of oral immunotherapy (OIT) with low or high doses of sesame protein (300 or 1200 mg, respectively) in children with a confirmed diagnosis of sesame allergy. The participants of current study will be recruited from patients who have accomplished their per-protocol participation in previous trial.
Patients will receive the same maintenance dose of sesame allergen, which was used in previous trial (300 or 1200 mg, respectively), for 32 weeks (+/-2 weeks). Then, OIT will be discontinued for 4 weeks with strict sesame avoidance. Subsequently, an open oral food challenge (OOFC) will be performed to assess the achievement of sustained unresponsiveness.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive daily a high dose of the sesame paste (1200 mg sesame protein) mixed with well-tolerated fruit mousse or bread.
Patients will receive daily a low dose of the sesame paste (300 mg sesame protein) mixed with well-tolerated fruit mousse or bread.
Time frame: Up to 9 months after starting maintenance phase
Percentage of patients tolerating their maintenance dose of sesame protein after a 4-week break in immunotherapy
Time frame: Up to 9 months after starting maintenance phase
Sustained unresponsiveness assessed as the highest tolerated dose of sesame protein at oral food challenge.
Time frame: Up to 9 months after starting maintenance phase
Number and severity of adverse events during OIT treatment and at OOFC will be assessed and compared between both groups.
Time frame: Up to 9 months after starting maintenance phase
Change in sesame serum immunoglobulin E (IgE) level and immunoglobulin G4 (IgG4) level at different time points: before immunotherapy, at the end of the maintenance phase and after a 4-week break in immunotherapy, assessed for each individual and compared between groups.
Time frame: Up to 9 months after starting maintenance phase
Difference in wheal diameter in skin prick tests (SPT) assessed between groups at the respective time points: before immunotherapy, at the end of the maintenance phase and after a 4-week break in immunotherapy.
Time frame: Up to 9 months after starting maintenance phase
Percentage of patients tolerating a single dose of 4000 mg of sesame protein after a 4- week break in immunotherapy.
Medical University of Warsaw
Other
Induction of Sustained Unresponsiveness to Sesame Using High- and Low-dose Sesame Oral Immunotherapy - Evaluation of Efficacy and Safety
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06369467
Food Allergy, Food Hypersensitivity
Tampa, Florida, United States
View Trial DetailsNCT06261554
Food Allergy, Food Hypersensitivity
Warsaw, Masovian Voivodeship, Poland
View Trial DetailsNCT01832324
Digestive System Diseases, Eosinophilia
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT05738798
Food Allergy, Food Hypersensitivity
Deventer, Overijssel, Netherlands
View Trial Details