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Clinical Trials/NCT05848986
NCT05848986Not yet recruitingNot Applicable

Study if the Presence of Functional FcERI/RII on the Surface of Human Blood Platelet

University Hospital, Strasbourg, France1 site in 1 country20 target enrollmentStarted: June 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
Presence of functionnal FcERI/RII receptors on the surface of blood platelets from allergic patients

Study Overview

Brief Summary

Anaphylactic shock is the most severe expression of immediate hypersensitivity reactions. The mechanisms leading to these reactions are still poorly understood and may involve platelets, especially in the most severe forms.

The IgE ( ImmunoglobulineE)-mediated mechanism, involving the FcERI(the high-affinity receptor for the Fc region of immunoglobulin E (IgE) receptor present on the surface of mast cells and basophilic cells, is the most common mechanism. The receptors FcERI and FcERII are also described as being present on the surface of blood platelets, which would imply their activation along with the other cells involved. However, studies showing the presence of the FcERI/RII receptors on blood platelets suffer from many biases.

The main objective of the research is to study whether the FcERI/RII receptors are present and functional on the surface of blood platelets from allergic patients.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age > 18 years-old
  • With a protein/drug allergy (hymenoptera, arachide, amoxicillin)
  • Confirmed by skin tests and/or challenge test
  • With specific IgEs

Exclusion Criteria

  • Patients who refuse to participate to this study
  • Patients unable to consent

Outcomes

Primary Outcomes

Presence of functionnal FcERI/RII receptors on the surface of blood platelets from allergic patients

Time Frame: 1 day

After confirmation of the allergy by a well conducted allergy workup

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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