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A retrospective cohort study on the factors influencing tracheostomy decannulation in patients with traumatic cervical spinal cord injury

The influencing factors on tracheostomy decannulation in patients with traumatic cervical spinal cord injury-A retrospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400085527
Enrollment
Unknown
Registered
2024-06-11
Start date
2023-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Spianl cord injury

Interventions

The tracheostomy was successfully decannulated group:none
The tracheostomy was not successfully decannulated group:none
non-tracheostomy group:none
Tracheostomy group:none

Sponsors

China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 86 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria for cervical spinal cord injury (CSCI). 2. CSCI related to trauma. 3. Patients with tracheostomy tube at admission or undergo tracheostomy during hospitalization. The severity of CSCI is classified according to the ASIA Impairment Scale developed by the American Spinal Injury Association (ASIA): A - Complete injury: no sensory or motor function preserved in the S4-S5 sacral segments. B - Incomplete injury: sensory function preserved below the neurological level and no motor function is preserved. C - Incomplete injury: motor function is preserved below the neurological level, and more than half of key muscles below the neurological level have a muscle grade less than 3. D - Incomplete injury: motor function is preserved below the neurological level, and at least half of key muscles below the neurological level have a muscle grade of 3 or more. E - Normal: sensory and motor function are normal.

Exclusion criteria

Exclusion criteria: 1. Non-traumatic cervical spinal cord injury (CSCI). 2. Hospitalization for reexamination or other treatments (such as pressure sores, spasms, neuropathic pain). 3. Clear evidence of brain function impairment. 4. Incomplete medical records or unclear diagnosis. 5. Hospital stay <48 hours.

Design outcomes

Primary

MeasureTime frame
factors for the tracheostomy was successfully decannulated;

Secondary

MeasureTime frame
factors for the tracheostomy;death rate;

Countries

China

Contacts

Public ContactLianjun Gao

China Rehabilitation Research Center, Beijing Bo'ai Hospital Capital Medical University, School of Rehabilitation Medicine

stlglj@126.com+86 188 0016 7065

Outcome results

None listed

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