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Effect of different ventilation modes on reintubation in patients with aortic dissection during spontaneous breathing trial

Effect of different ventilation modes on reintubation in patients with aortic dissection during spontaneous breathing trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076042
Enrollment
Unknown
Registered
2023-09-22
Start date
2023-09-30
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

Aortic dissection

Interventions

Group A:After the patient was evaluated by the physician, pressure support ventilation of 8cmH2O was applied for 30min during SBT.
Group B:After evaluation by the doctor, pressure support ventilation of 8cmH2O was used for 30min during SBT, and MV was reconnected for 1h after successful SBT.
Group C:After the patient was evaluated by the physician, the patient was provided with T-mode ventilation for 2 hours during SBT.
Group D:After the patient was evaluated by the physician, the patient was provided with T-mode ventilation for 2 h during SBT and then reconnected to MV for 1h after successful SBT.

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) age =18 years old; (2) patients with a definite diagnosis of aortic dissection; (3) Informed consent was obtained from patients and their families.

Exclusion criteria

Exclusion criteria: (1) The patient was complicated with severe respiratory diseases; (2) complicated with other major dysfunction, such as severe intracranial disease; (3) pregnant women;

Design outcomes

Primary

MeasureTime frame
Rate of reintubation;

Secondary

MeasureTime frame
Success rate of extubation; 7/5000 Length of ICU stay;Mortality in the ICU;

Countries

China

Contacts

Public ContactXiaoqin Liao

Fujian Medical University Union Hospital

17850858308@163.com+86 178 5085 8308

Outcome results

None listed

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