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Wean earlier and automatically with new technology: a multicentre, pilot randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43760151
Enrollment
90
Registered
2006-01-30
Start date
2006-05-30
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Weaning intubated adults from invasive mechanical ventilation Respiratory Invasive mechanical ventilation

Interventions

Automatic (computer-driven) weaning versus protocolized weaning

Sponsors

Physician Services Incorporated (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are invasively ventilated for at least 24 hours

Exclusion criteria

Exclusion criteria: 1. Age < 16 years 2. Tracheotomy 3. Pregnancy 4. Do not intubate (DNI) or do not resuscitate (DNR) patients 5. Planned extubation on the day of study inclusion 6. Planned surgery or procedures within 48 hours of randomization

Design outcomes

Primary

MeasureTime frame
Compliance with the weaning and sedation protocols

Secondary

MeasureTime frame
1. Acceptance of the weaning and sedation protocols 2. Weaning and Intensive Care Unit (ICU) related-complications 3. Time to successful completion of a Single Breath Test (SBT) and extubation

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 2, 2026