Anaphylaxis

8

Review clinical trials related to Anaphylaxis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Diagnosis and Allergen Identification of Perioperative Anaphylaxis

Perioperative anaphylaxis may lead to fatal respiratory and/or circulatory events, yet both clinical diagnosis and management are challenging. Serum tryptase is an indicator that can provide important retrospective diagnostic value for anaphylaxis. Another key point in perioperative anaphylaxis management is to identify the allergens, and thus avoid re-exposure during later perioperative management. Skin testing is an important way to identify allergens.

Participants needed: 115
Trial details
Age: 2+Biological sex: AllType: ObservationalSponsor: Peking University First HospitalUpdated: Jun 18, 2026Locations: 6
Eligibility criteria

Aged 2 years or over; [+1]

Refuse to participate; [+1]

Status: Recruiting

Effects of Inhaled Epinephrine on Systemic Allergic Reactions During Allergy Testing, Immunotherapy or Oral Challenges

The goal of this exploratory study is to evaluate the effects of inhaled epinephrine in subjects, who may not be eligible for the GHL-101 trial, and who are experiencing systemic allergic reaction (SAR) that occur following allergy testing, subcutaneous immunotherapy (SCIT), oral challenges (with food and/or drug) or oral immunotherapy (OIT).

Participants needed: 100
Trial details
Phase: Phase 1Age: 12+Biological sex: AllType: InterventionalSponsor: Dr. George LuciukUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Males or females, aged ≥ 12 years with known or suspected allergen sensitivity w... [+2]

Known reaction or sensitivity to epinephrine or any of the ingredients of inhale... [+6]

Status: Recruiting

Steroid Use in Treatment of Allergic Reactions to Food

In this study, the investigators want to find out whether a specific medication commonly used for severe allergic reactions is really necessary. When children have allergic reactions to foods, they are often given medications to relieve the symptoms. In addition to adrenaline and antihistamines, steroids are frequently administered in German-speaking Switzerland. However, it is unclear whether steroids are really helpful in this situation. To investigate this, the investigators are comparing two groups: one group receives additional steroids, and the other does not. Which treatment a participant receives is decided randomly, like flipping a coin. The study takes place during a pre-scheduled provocation test at the clinic. If an allergic reaction occurs, the usual emergency medications will be administered. Doctors will closely monitor how the reaction develops. No additional tests or visits are required. The results of this study could help improve allergy treatment in the future.

Participants needed: 160
Trial details
Phase: Phase 4Age: 6-18Biological sex: AllType: InterventionalSponsor: Johannes TrueckUpdated: Jan 27, 2026Locations: 2
Eligibility criteria

suspected or confirmed IgE-mediated food allergy

Non-IgE mediated food allergies [+3]

Status: Recruiting

Analysis of the Role of IgE Proteoforms in Health and Disease

The goal of this observational study is to evaluate the role of IgE proteoforms in healthy volunteers and in patients with type I allergy, patients with chronic spontaneous urticaria, patients with a recent history of anaphylaxis, patients with mastocytosis, patients with hereditary alpha tryptasemia, patients with X-linked agammaglobulinemia (XLA), and patients undergoing desensitization for venom or medication allergy.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: KU LeuvenUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

CSU and type I allergic diseases (including anaphylaxis and desensitization), at... [+1]

Absence of informed consent [+1]

Status: Recruiting

A Registry for the Food Allergy Community

The FARE Patient Registry will serve as a prospective, observational food allergy reporting system that stores detailed health and other basic information about patients' real-world experiences with food allergies, to encourage open sharing of de-identified data and participation in clinical trials. The FARE Patient Registry intends to make and support scientific discoveries by enabling the food allergy community to participate directly in research.

Participants needed: 23,000
Trial details
Biological sex: AllType: ObservationalSponsor: Food Allergy Research & EducationUpdated: Mar 12, 2025Locations: 1Duration: 5 Years
Eligibility criteria

Individuals with diagnosed food allergy

Individuals without food allergy

Status: Recruiting

Acquisition and Long-term Observation of Patients With Severe Allergic Reactions

The Anaphylaxis Registry aims to assess data in a standardized form about symptoms, triggers, cofactors and therapy management from patients who experienced an anaphylactic reaction. This should improve diagnosis and long-term management of these life-threatening allergic reactions.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: Charite University, Berlin, GermanyUpdated: Aug 21, 2024Locations: 1Duration: 1 Day
Eligibility criteria

Anaphylactic reaction within the past 12 months

Status: Recruiting

Use of Dexamethasone in Prevention of the Second Phase or a Biphasic Reaction of Anaphylaxis

Anaphylaxis is an acute serious allergic reaction, with multi-organ system manifestations caused by the release of chemical mediators and it is potentially fatal . Between 5% and 14% of patients may experience a recurrence of anaphylaxis 8-12 hours after the initial presentation, called biphasic (late-phase) . The mainstay of treatment for children experiencing anaphylaxis remains adrenaline and H1-antihistamines. Corticosteroids are not life-saving and do not have an immediate effect on the symptoms of anaphylaxis but may help reduce or prevent a biphasic "late phase" reaction . The aim of this study is to compare the efficacy of oral glucocorticoids in prevention of the second phase or biphasic reaction of anaphylaxis, as compared to placebo in children, presenting to the pediatric emergency department (PEC Al-Sadd) with mild to moderate anaphylaxis (Prospective Study). Patients will be randomized to either one of the two treatment: Treatment 1: Dexamethasone 0.6mg/kg oral. Treatment 2 : Placebo All patients will be urgently treated for anaphylaxis according to guideline protocol. Enrolled patients will be given one of the study medications orally, and he /she will observe in the observation room with cardiac monitor and close monitoring by nurse. The treating physician will discharge patient when he/she looks well, breathing comfortably, has oxygen saturation \>94%, stable blood pressure and no gastrointestinal or neurological manifestation. Discharge patients will be sent home on anti-histamine (cetirizine) for 5days. All patients will be followed up for one week post discharge by a phone call asking about the general condition, relapse of symptoms, or need for readmission.

Participants needed: 210
Trial details
Phase: Phase 1Age: 3-14Biological sex: AllType: InterventionalSponsor: Hamad Medical CorporationUpdated: Aug 14, 2024Locations: 1
Eligibility criteria

All patients 3 monthes-14years presenting to the Pediatric Emergency Department...

Status: Recruiting

Acutelines: a Large Data-/Biobank of Acute and Emergency Medicine

Research in acute care faces many challenges, including enrollment challenges, legal limitations in data sharing, limited funding, and lack of singular ownership of the domain of acute care. To overcome some of these challenges, the Center of Acute Care of the University Medical Center Groningen in the Netherlands, has established a de novo data-, image- and biobank named "Acutelines". Acutelines is initiated to improve recognition and treatment of acute diseases and obtain insight in the consequences of acute diseases, including factors predicting its outcome. Thereby, Acutelines contributes to development of personalized treatment and improves prediction of patient outcomes after an acute admission.

Participants needed: 35,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Medical Center GroningenUpdated: Jun 13, 2024Locations: 1Duration: 5 Years
Eligibility criteria

Triaged as one of highest two triage categories (red or orange) according to the... [+12]

Referred for organ transplantation as recipient [+2]