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Anaphylaxis clinical trials

View clinical trials related to Anaphylaxis.

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NCT ID: NCT06405399 Completed - Clinical trials for Anaphylactic Reaction

Design, Implementation and Evaluation of the Guided Observer Role in Clinical Simulation

Start date: May 10, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to assess the effectiveness of the guided observed role in a simulation learning programme for nursing students in acquiring the competence (knowledge, skills and attitudes) to care for patients affected by anaphylactic situations. This will be achieved by comparing the participants' simulation roles with the guided observed role. The design was that of an exploratory randomised controlled trial. The variables employed to assess the efficacy of the intervention were competence and its associated attributes. These were measured using a ten-question multiple-choice test to assess knowledge; the simulation performance assessment using the Creighton Simulation Evaluation Instrument to assess skill; the learner's perception of the simulation's effectiveness in meeting their learning needs, through the Simulation Effectiveness Tool Modified (SET-M). Furthermore, the extent to which reflective thinking was achieved during the simulation was evaluated using the Self-Debriefing Reflection Rubric. Additionally, the students' perceptions of their role were assessed through seven open-ended questions.

NCT ID: NCT06316414 Completed - Asthma in Children Clinical Trials

Omalizumab in Severe Asthmatics With Food Allergy

OSAFA
Start date: January 1, 2018
Phase:
Study type: Observational

A prospective assessment of the impact of Omalizumab in terms of efficacy, safety, and quality of life (FA-QoL) in patients with moderate/severe asthma and history of anaphylaxis to peanut, tree nuts, fish, egg, milk, and/or wheat. Evaluation of the trend of total and specific IgE during Omalizumab treatment.

NCT ID: NCT06205134 Completed - Anaphylaxis Clinical Trials

Comparative Bioavailability of Intranasal Epinephrine

Start date: August 22, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

A Study to Compare the Bioavailability of Epinephrine following a Single Nasal Dose of FMXIN002 Microspheres Powder 3.6 mg, and 4mg with EpiPen 0.3mg Intramuscular Injection in Healthy Adults

NCT ID: NCT05894499 Completed - SARS-CoV-2 Clinical Trials

Post-Marketing Safety Study in Japan of Shock and Anaphylaxis After Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) mRNA-1273 COVID-19 Vaccine in Persons in at High Risk of Severe COVID-19

Start date: November 15, 2022
Phase:
Study type: Observational

The goal of this study is to confirm the onset status of hypersensitivity reactions including shock and anaphylaxis observed after vaccination with this drug in persons with underlying diseases who are considered to have a high risk of severe exacerbation of COVID-19 and explore risk factors.

NCT ID: NCT05152901 Completed - Clinical trials for Anaphylactic Reaction

Study of Inhaled Epinephrine and Intramuscular Epinephrine Administered to Healthy Adults

Start date: January 6, 2022
Phase: Phase 1
Study type: Interventional

This is a study to determine the relative bioavailability of inhaled epinephrine compared with 0.3mg epinephrine administered IM in healthy male and female participants.

NCT ID: NCT05038904 Completed - Food Allergy Clinical Trials

Preventing Anaphylaxis With Acalabrutinib

Start date: December 16, 2021
Phase: Phase 2
Study type: Interventional

Food allergy is a potentially life-threatening condition, and its prevalence continues to increase despite public health efforts. There are currently no known therapies that can reliably prevent food-induced anaphylaxis. This is an open-label study designed to determine the ability acalabrutinib to prevent signs and symptoms of anaphylaxis during an oral food challenge in food-allergic adults.

NCT ID: NCT04825106 Completed - Diagnostic Error Clinical Trials

Diagnostic Errors in Anaphylactic Shock

ANASim
Start date: January 1, 2008
Phase: N/A
Study type: Interventional

Diagnostic accuracy and quality of management in anaphylactic shock is assessed in three conditions: expected, unexpected with no distractor, unexpected with distractor

NCT ID: NCT04696822 Completed - Anaphylaxis Clinical Trials

Bioavailability of Nasal Epinephrine

Start date: November 1, 2020
Phase: Phase 1
Study type: Interventional

A Study to Compare the Bioavailability of Epinephrine following a Single Nasal Dose of FMXIN002 Microspheres Powder with Epinephrine 0.3 mg Intramuscular Injection in Adult Subjects with Seasonal Allergic Rhinitis with and without Nasal Allergen Challenge

NCT ID: NCT04360213 Completed - Allergy Clinical Trials

Advanced Multimodal Wireless Vital Signs Monitoring for Patients With Asthma and Anaphylaxis

Start date: June 1, 2021
Phase:
Study type: Observational

The primary objective of this study is to assess the function and reliability of a non-invasive, skin-like electronic sensor. We hypothesize that this skin sensor will address an unmet need to wirelessly, noninvasively, and rapidly assess critical vital signs and other measures essential to healthcare monitoring for patients with asthma and anaphylaxis.

NCT ID: NCT04290507 Completed - Anaphylaxis Clinical Trials

Epidemiology and Outcome of Anaphylactic Shocks Admitted to Intensive Care Unit

ANAPHYLASHOCK
Start date: January 1, 2017
Phase:
Study type: Observational

Anaphylaxis is a severe life-threatening reaction following exposure to an antigen. Its incidence is progressively increasing in the general population over years, accompanied with an increased number of hospitalizations. Although rare, this condition is often associated with a significant morbidity and mortality. The mortality rate has been recently estimated at 0.84 (95% CI, 0.79 to 0.88) per million per year in the French adult population. Age, chronic medication and cardiac or pulmonary comorbidities have been reported to increase the risk of a severe reaction. Obesity, age and cardiovascular comorbidities have been identified as risk factors for fatal anaphylaxis. However, the risk factors for death after ICU admission have not been elucidated yet.