Effects of a postextubation respiratory failure prevention program on postextubation respiratory failure and clinical outcomes among critically ill medical patients

Effects of a Postextubation Respiratory Failure Prevention Program on postextubation respiratory failure and clinical outcomes among critically ill medical patient

Status

Unknown

Phases

Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20231017003

Enrollment

100

Registered

2023-10-17

Start date

2023-06-06

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Post-extubation respiratory failure Postextubation, respiratory failure, critical ill patient

Interventions

standard of care,Postextubation respiratory failure prevention program

Experimental Procedure/Surgery,Experimental Procedure/Surgery

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: All patients aged over 18 years who were admitted to ICU and submitted to IMV through an endotracheal tube for more than 24 hours were eligible for inclusion.

Exclusion criteria

Exclusion criteria: Patients likely to require tracheostomy, having accidental extubation or self-extubation, and not meet- ing the eligibility criteria for extubation were excluded.

Design outcomes

Primary

Measure	Time frame
Postextubation respiratory failure 72 hours Incidence of Postextubation respiratory failure	—

Secondary

Measure	Time frame
reintubation 72 hours Incidence of reintubation	—

Countries

Thailand

Contacts

Public ContactTeerawat Somkamsri

Faculty of Medicine, Khon Kaen University

teeraso@kku.ac.th0863878005

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026