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Perioperative respiratory adverse events risk assessment in children: development of a risk prediction tool

Perioperative respiratory adverse events risk assessment in children: development of a risk prediction tool

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038100
Enrollment
Unknown
Registered
2020-09-10
Start date
2020-10-12
Completion date
Unknown
Last updated
2020-11-24

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

Conditions

Perioperative respiratory adverse events

Interventions

respiratory adverse events group vs no respiratory adverse events group:no intervention

Sponsors

Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: (1) ASA level 1~3; (2) Aged <=18 years; (3) Medical intervention, elective surgery or emergency non-cardiac general anesthesia is proposed.

Exclusion criteria

Exclusion criteria: (1) Congenital heart disease; (2) Intubation or tracheotomy; (3) Pulmonary cystic fibrosis; (4) Neuromuscular diseases, cerebral palsy, seizures; (5) Thoracic, upper abdominal or neurosurgical operations; (6) Parents with severe hearing or visual impairment who cannot communicate effectively with doctors; (7) Unable to understand the content of the scale and reject the participants.

Design outcomes

Primary

MeasureTime frame
laryngospasm;bronchospasm;Oxygen saturation is below 95 percent;Persistent cough;wheeze;—

Countries

China

Contacts

Public ContactZhang Yueying

Xuzhou Medical University

zyy0218@126.com+86 13815310789

Outcome results

None listed

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