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Japanese Epidemiologic Study for Perioperative Anaphylaxis

Japanese Epidemiologic Study for Perioperative Anaphylaxis - Japanese Epidemiologic Study for Perioperative Anaphylaxis (JESPA)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000035350
Enrollment
150
Registered
2018-12-25
Start date
2019-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

anaphylaxis

Interventions

None listed

Sponsors

Gunma University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The patient whose consent has been obtained in writing with respect to participation in this study 2) The patient showing Grade 2 or severer anaphylactic reactions during perioperative period. In the medical institutions conducting research A only, the subject will be patient showing Grade 3 or severer anaphylactic reactions

Exclusion criteria

Exclusion criteria: 1) The patient who did not give consent for participation 2) The patient who use or have a plan to use unapproved drugs such as investigational drugs 3) The patient to whom a doctor judged inappropriate for participating in this study

Design outcomes

Primary

MeasureTime frame
Identification of causative drug(s) of perioperative anaphylaxis

Secondary

MeasureTime frame
Incidence and severity of perioperative anaphylaxis

Countries

Japan

Contacts

Public ContactTomonori Takazawa

Gunma University Hospital Intensive Care Unit

takazawt@gunma-u.ac.jp027-220-8698

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026