Evaluation of the safety and efficiency of two decannulation protocol in patients with severe brain injury who underwent tracheostomy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300076558

Enrollment

Unknown

Registered

2023-10-11

Start date

2023-11-01

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Tracheostomy decannulation

Interventions

Prospective observational study: All patients in the experimental group will undergo post-admission routinely screening to determine decannulation readiness according to an decannulation protocol base

Historical control study: All patients in the experimental group will undergo post-admission routinely screening to determine decannulation readiness according to capping trial

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: ?age =18y;?GCS=8;?: patients who can tolerate tracheostomy tube deflation

Exclusion criteria

Exclusion criteria: ? Unable to cooperate with fiberoptic endoscopy examination; ? informed consent was not obtained.

Design outcomes

Primary

Measure	Time frame
Time to decannulation;	—

Secondary

Measure	Time frame
Decannulation rate;Decannulation failure rate;Incidence of respiratory compliation ;	—

Countries

China

Contacts

Public ContactSong Lu

Fuxing Hospital, Capital Medical University

18963876@qq.com+86 150 1085 2973

Outcome results

None listed

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