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An observational study of adverse events after general anesthesia in women's and children's Hospital

An observational study of adverse events after general anesthesia in women's and children's Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091291
Enrollment
Unknown
Registered
2024-10-24
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

None listed

Interventions

Adult Group:NA
Child Group:NA

Sponsors

Shunyi Maternal and Children's Hospital of Beijing Children's Hospital, Beijing
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. 8 months 2024-6 months 2024 to PACU after general anesthesia patients 2. Age > 0 years 3. Sign the informed consent form

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1. Serious Mental Illness 2. Severe Brain Disease 3. Deaf-mutes 4. Other serious systemic diseases

Design outcomes

Primary

MeasureTime frame
Adverse reactions;—

Secondary

MeasureTime frame
Adverse event handling in the PACU;The medication of anesthesia, adverse events and management during operation;PACU dwell time;—

Countries

China

Contacts

Public ContactLiu Guoliang

Shunyi Maternal and Children's Hospital of Beijing Children's Hospital, Beijing

liuguoliang0@163.com+86 138 1012 0027

Outcome results

None listed

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