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Cross sectinal study during intrahospital transports to diagnostic tests of patients in the intensive care unit

Adverse events during intrahospital transports to diagnostic tests of patients in the intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCS-12002661
Enrollment
Unknown
Registered
2012-11-05
Start date
2012-11-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Critically disease

Interventions

Group One:No

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: 1. All patients in the intensive care unit who required intrahospital transport to accept diagnostic tests during the study period could be included; 2. Written informed consent should be obtained from the patients, their guardians or family members.

Exclusion criteria

Exclusion criteria: There is no exclusion criteria.

Design outcomes

Primary

MeasureTime frame
Rate of adverse events;—

Countries

China

Contacts

Public ContactKaijiang Yu
drkaijiang@sohu.com+86 13303608899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026