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Recruiting NCT04438525

Is the BAT Inhibition Able to Replace Sting Challenges? (BATIRS)

No phase Interventional Vespid Venom Allergy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: sting challenge, blood donation.
Who it may be relevant to
Registry conditions: Vespid Venom Allergy. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Austria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Is the BAT Inhibition Able to Replace Sting Challenges?

Overview

Insect venom allergy is the major cause for severe allergic reactions in Europe. Wasps and honeybees are responsible for the majority of these allergic reactions. Symptoms range from generalized skin symptoms (wheals, swellings) to respiratory or cardiovascular problems such as asthma, dizziness, loss of consciousness, or cardiac arrest. The regular administration of insect venom ('venom immunotherapy') over up to 5 years is a well-established therapy, providing long-term protection from further systemic sting reactions in the majority of patients. However, there is no laboratory test which is able to identify patients who will still react to an insect sting. The only reliable method available is stinging patients with living insects ('sting challenges'). The key issue is that only few centers in Europe perform sting challenges and many patients have no access to these tests. Therefore, it is of utmost importance to find a method which is able to identify patients who are still at risk for future allergic sting reactions. The inhibition of the basophil activation test (BAT) could be a potential method to monitor the effectiveness of immunotherapy. Basophils are cells which are activated in acute allergic reactions. The basophil activation of blood donors with vespid venom allergy can be measured after adding sera from allergic patients undergoing immunotherapy. In a preliminary study we found that the activation of basophils could be inhibited in all patients treated with vespid venom, however, results must be confirmed in a larger study. In this study, a total of 219 patients with vespid venom allergy will be included. Those patients who are receiving or who have already finished venom immunotherapy will be sting challenged and blood samples will be taken to perform BAT inhibition experiments. At the same time, donors with confirmed vespid venom allergy, who have not undergone immunotherapy, will be recruited for a blood donation, which is necessary for the BAT inhibition tests. If results of the preliminary study could be confirmed, the BAT inhibition will facilitate monitoring the effectiveness of venom immunotherapy and patients would benefit from an early detection of lacking tolerance and consequently from the increased venom dose preventing future life threatening systemic sting reactions.

Interventions

  • Diagnostic test sting challenge
    At the Moment, sting challenges are the only reliable method to identify patients who are not protected by insect venom immunotherapy.
  • Other blood donation
    To perform BAT Inhibition Tests, blood samples of patients with confirmed vespid venom allergy, who have not undergone venom immunotherapy, are necessary.

Primary outcome measures

  • Outcome sting challenge vs. BAT Inhibition test [Time frame: 4 hours]

Eligibility criteria

Inclusion criteria

  • Legally competent male and female subjects who are currently treated or who have been treated with vespid venom immunotherapy
  • Age ≥18 and ≤70 years
  • Written consent of the participant after being informed

Exclusion criteria

  • Pregnancy
  • Autoimmune disease
  • Uncontrolled cardiovascular disease
  • Uncontrolled asthma

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Diagnostic

Study locations

Austria · 1 center
  • Department of Dermatology and Venerology, Medical University of Graz — Graz

Identifiers

NCT: NCT04438525 · 30-381 ex 17/18 (BATIRS)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗