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Incidence of adverse events during intra-hospital transport of high-risk critically ill patients and the related risk factors: a medical records based retrospective study

Incidence of adverse events during intra-hospital transport of high-risk critically ill patients and the related risk factors: a retrospective, single center study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054511
Enrollment
Unknown
Registered
2021-12-19
Start date
2021-12-27
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

critical illness

Interventions

Case series:No

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients who required intra-hospital transport to perform diagnostic or therapeutic procedures during the study period were included.

Exclusion criteria

Exclusion criteria: 1. Aged < 18 years; 2. During the in-hospital transfer process, the transfer monitor was not used for vital signs monitoring; 3. Lack of blood gas analysis data before and after transport.

Design outcomes

Primary

MeasureTime frame
incidence of adverse events;—

Countries

China

Contacts

Public ContactJia Liu

The Second Affiliated Hospital of Harbin Medical University

jialiu179@163.com+86 13845076587

Outcome results

None listed

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