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A case records based multi-center retrospective analysis of severe anesthesia-related perioperative adverse events

A case records based multi-center retrospective analysis of severe anesthesia-related perioperative adverse events

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018056
Enrollment
Unknown
Registered
2018-08-28
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

Anesthesia-related perioperative adverse events

Interventions

Case series:none

Sponsors

Department of Anesthesiology, Union hospital, Tongji medical college, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 99 Years

Inclusion criteria

Inclusion criteria: The patients with severe adverse events in 24 hours after anesthesia began

Exclusion criteria

Exclusion criteria: 1. Information of the case was missing or incomplete; 2. Patients who have not signed the informed consent form.

Design outcomes

Primary

MeasureTime frame
cardiac arrest;death;delayed recovery;hypothermia;local anesthetic intoxication;anaphylaxis;malignant hyperthermia;laryngospasm&asthma;difficult airway;Unplanned transfer to ICU;Non-scheduled secondary intubation;atelectasis;—

Secondary

MeasureTime frame
age;gender;ASA;high;kg;surgical site;hospital level;—

Countries

China

Contacts

Public ContactYao Shanglong

Department of Anesthesiology, Union hospital, Tongji medical college, Huazhong University of Science and Technology, Wuhan, China

ysltian@163.com+86 13886128437

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026