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临床试验/NCT06256146
NCT06256146招募中不适用

Investigating Modified Protocols of Oral Immunotherapy to Validate Efficacy and Safety

McGill University Health Centre/Research Institute of the McGill University Health Centre1 个研究点 分布在 1 个国家目标入组 360 人开始时间: 2022年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
360
试验地点
1
主要终点
Rate of anaphylaxis in different Oral Immunotherapy protocols

研究概览

简要总结

Protocols for Oral Immunotherapy (OIT) for the main food allergens have been recently incorporated in clinical practice for food allergies and their clinical benefits have been acknowledged in European and Canadian official guidelines. There has been some reluctance in both clinicians and patients to implement these therapies, primarily because of the risk of allergic reactions during the desensitization process. This study will investigate if protocols using low doses of a food allergen or processed versions of the allergen can be both effective in conferring desensitization while inducing fewer allergic symptoms during the desensitization process.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • A history suggestive of immediate allergy to the food. A convincing clinical history of an IgE mediated reaction to a specific food will be defined as a minimum of 2 mild signs/symptoms or 1 moderate or 1 severe sign/symptom that was likely IgE mediated and occurred within 120 minutes after ingestion or contact
  • The presence of at least one of the following confirmatory tests:
  • Positive SPT to the culprit food allergen (weal diameter 3 mm larger than that of the normal saline control). The allergens used will be commercial extracts of the foods (Omega Labs, Toronto, Ontario).
  • Detection of serum specific IgE (>0.35 kU/L) to the culprit food or any of its proteins, measured by fluorescence enzyme immunoassay (Phadia, CAP System, Uppsala, Sweden).

排除标准

  • Patients who have uncontrolled respiratory disease (asthma, cystic fibrosis, etc.)
  • Patients who present with intercurrent disease active at the time of starting desensitization.
  • Non IgE mediated or non-immunological adverse reactions to milk or peanuts.
  • Malignant or immunopathological diseases and/or severe primary or secondary immune deficiencies.
  • Patients receiving oral immunosuppressor therapy.
  • Patients receiving β-blockers (including topical formulations), or who receive daily doses of NSAIDs, aspirin or ACE inhibitors for cardiac issues.
  • Associated diseases contraindicating the use of epinephrine: cardiovascular disease, severe hypertension or hypotension.
  • Patients diagnosed with eosinophilic gastrointestinal disorders, including patients with a history of antacid use for reflux related to food impaction or with a history of esophageal spasm.
  • Patients already tolerating processed/cooked forms of the food (e.g.,baked goods with milk).

研究组 & 干预措施

Modified Protocol - Low Dose Arm

Experimental

Subjects will progress through desensitization to a low maintenance dose - 120 mg of crushed peanut, 50 ml of milk or 300 mg of egg powder.

干预措施: Food allergy desensitization / Oral Immunotherapy (Other)

Standard Protocol - High Dose Arm

Experimental

Subjects will progress through desensitization to a high maintenance dose - 1200 mg of crushed peanut, 200 ml of milk or 1200 mg of egg powder.

干预措施: Food allergy desensitization / Oral Immunotherapy (Other)

Modified Protocol - Cooked/Transformed Allergen Arm

Experimental

Subjects will begin desensitization with cooked versions of the allergen (muffins in the case of egg and milk) or transformed versions (Bamba puffs for peanut). They will progress up to a full muffin or 4 Bamba puffs (for egg/milk and peanut respectively). Once subjects have reached these doses, they will transition to doses of pure allergen. They will then progress to the same top dose as subjects in the High Dose Arm.

干预措施: Food allergy desensitization / Oral Immunotherapy (Other)

结局指标

主要结局

Rate of anaphylaxis in different Oral Immunotherapy protocols

时间窗: 3 years

Do participants in the different study arms experience similar rates of anaphylaxis during their participation in the study? Anaphylaxis is defined as an allergic reaction to the food the subject is allergic to, that involves symptoms in two of the following organ systems: skin, respitratory, gastro-enterologic or neurologic.The Consortium for Food Allergy Research (CoFAR) grading scale will be used for assessing severuty of allergic symptoms

次要结局

  • Efficacy of different Oral Immunotherapy protocols(3 years)

研究者

发起方
McGill University Health Centre/Research Institute of the McGill University Health Centre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Moshe Ben-Shoshan

Assistant Professor of Pediatrics

McGill University Health Centre/Research Institute of the McGill University Health Centre

研究点 (1)

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