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The study for identifying the antigen of culprit agents of perioperative anaphylaxis

Not Applicable
Conditions
Anaphylaxis
Registration Number
JPRN-UMIN000044591
Lead Sponsor
Gunma University Hospital, Department of Anesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Those who the doctor deems inappropriate for participating in this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Basophil activation tests conducted 4 to 6 weeks after anaphylaxis
Secondary Outcome Measures
NameTimeMethod
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