New study aims to spot Life-Threatening allergies in the operating room
NCT ID NCT03918772
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 145 people who had an allergic or non-allergic reaction during surgery. Researchers wanted to find out which signs, like skin changes or heart rate, could tell the difference between a true allergy and a non-allergic reaction. The goal is to help doctors treat dangerous allergic reactions faster and more accurately.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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145 people
The number who actually took part.
- Started
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Nov 2018
- Finished
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Mar 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients having experienced a perioperative immediate hypersensitivity where the allergological assessment was performed by the collaborators of this study
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Patients having experienced a perioperative immediate hypersensitivity (including the obstetrical setting) according to one grade of the Ring and Messmer clinical scale, for whom: * The clinical history is known and has been related to perioperative immediate hypersensitivity; * The biological assessment including plasma histamine and/or tryptase (and serum IgE when available) was performed after the onset of immediate hypersensitivity according to current guidelines; * The allergological assessment including skin tests performed by the collaborators of this study was carried out according to current guidelines in surviving patients Exclusion criteria: • Patients who decline to be involved in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Assistance Publique-Hôpitaux de Paris
Paris, 75004, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.