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To construct a prediction model for laryngospasm under intravenous anesthesia in children based on preoperative risk factors

To construct a prediction model for laryngospasm under intravenous anesthesia in children based on preoperative risk factors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120045
Enrollment
Unknown
Registered
2026-03-09
Start date
2026-03-16
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Laryngospasm in pediatric anesthesia

Interventions

Observation group(Pediatric Intravenous Anesthesia):N/A

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 7 Years

Inclusion criteria

Inclusion criteria: 1.Pediatric patients aged 0–7 years who are scheduled to undergo fundus examination for retinoblastoma under intravenous anesthesia. 2.Legal guardians have provided informed consent and signed the informed consent form. 3.American Society of Anesthesiologists (ASA) physical status classification ?–?. 4.Complete clinical data are available, and the patients can cooperate with the collection of perioperative data.

Exclusion criteria

Exclusion criteria: 1.Severe adverse events (e.g., anaphylactic shock) occurred during the procedure, necessitating the termination of surgery or examination. 2.Incomplete data collection (with = 3 key indicators missing). 3.Legal guardians requested withdrawal from the study midway.

Design outcomes

Primary

MeasureTime frame
Occurrence of Laryngospasm in Children During Intravenous Anesthesia and Recovery Period;

Countries

China

Contacts

Public ContactGuanghui An

Shanghai General Hospital

gh_An@163.com+86 21 63240090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026