Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
NCT Number: NCT04222491
This is an open label observational single center study of clinical food oral immunotherapy outcomes with biomarker samples and participant and/or caregiver-completed questionnaires in participants between 6 months and 65 years of age with IgE-mediated peanut allergy undergoing food oral immunotherapy.
This study is active but is not currently recruiting participants.
6 month–65 year
All sexes
Observational
Boston, Massachusetts, 02114, United States
In this research study the investigators want to learn more about the experience of participants with peanut allergy and their caregivers undergoing food oral immunotherapy (OIT) for peanut allergy. Food oral immunotherapy (OIT) is a treatment for individuals with a food allergy to reduce the body's allergic response to the food allergen, resulting in fewer symptoms. The treatment is also called desensitization. An individual becomes desensitized to the food allergen by ingesting small amounts of the food that are slowly increased. Over time, this helps the body's immune system become used to the food so that it no longer causes an allergic reaction. By desensitizing to peanut, it may lower the risk of life-threatening allergic reactions and cause a decreased sensitivity to peanut. The investigators specifically want to learn more about the effects of food OIT on quality of life and other outcomes important to participants with peanut allergy and their caregivers and to ultimately develop tests to predict who may respond favorably to food OIT.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Peanut oral immunotherapy for peanut allergy
Other names: Peanut flour, Peanut allergen powder
Time frame: 2 years
Feasibility analysis as assessed by the proportion of participants who tolerate the maintenance dose in a dichotomous manner
Time frame: 4 years
Change in quality of life scores from baseline assessment to end of treatment assessment using the Food Allergy Quality of Life Questionnaire (FAQLQ) total score. The FAQLQ total and domain scores range from 1-7 where 1 was the best possible score (i.e. fewest problems or better health related quality of life) and with the total score being the average of the domain scores. The domains include Emotional Impact, Social and Dietary Restrictions, and Food Anxiety.
Time frame: 4 years
Change in peanut specific serum immunoglobulin E (IgE) [in kilo-units per liter (kU/L) or international units per milliliter (IU/mL)] from baseline to end of treatment
Time frame: 4 years
Change in skin prick test wheal diameter measurement in millimeters to peanut extract from baseline to end of treatment
Time frame: 4 years
Desensitization to peanut as assessed by cumulative tolerated dose
Time frame: 4 years
Safety analysis as assessed by patient-reported or observed allergic symptoms that will be analyzed and tabulated
Massachusetts General Hospital
Other
Outcomes of Clinical Food Oral Immunotherapy for Peanut Allergy
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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.
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