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Utility of a Weaning Protocol in ICU

Non Pharmacological Randomized Clinical Trial Designed to Evaluate the Difference of the Duration of Weaning Process From the Ventilator Between Protocol-driven Weaned Patients and Clinical-driven Weaned Patients.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01877850
Acronym
WEAN
Enrollment
60
Registered
2013-06-14
Start date
2013-05-31
Completion date
2014-05-31
Last updated
2015-04-23

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

Conditions

Weaning Failure

Brief summary

The purpose of this study is to evaluate the difference of the duration of weaning process from the ventilator between protocol-driven weaned patients and clinical judgment driven weaned patients.

Detailed description

All patients with prolonged weaning and who required tracheostomy are enrolled in the study. These patients are randomized as Case or Control by a computer program. Patients can start the weaning process when the acute phase of the respiratory failure has been resolved and pressure support ventilation was setted. For all this patients are calculated modified-BWAP(BWAP-M) and TOBIN indexes. The Case patients started the weaning protocol process only if BWAP-M value is more than 15 or BWAP-M 10-15 with Tobin index \< 100. If not, the BWAP-M and Tobin will be calculated every day. The Control patients will start weaning by clinical judgement even if the BWAP-M value is less than 10. For all patients are calculated: the duration of weaning process, the ICU length of stay and the duration of the mechanical ventilation.

Interventions

Reduction of pressure support ventilation (PSV) by 2cmH2O at a time to a maximum of 4cmH2O per day. When a patient was able to tolerate PSV less than 8 cmH2O for at least 120 minutes, the nurses started to reduce End Expiratory Positive Pressure (PEEP) by 2cmH2O at a time to a maximum of 4cmH2O per day. When a patient was able to tolerate PSV less than 8 cmH2O with PEEP less than 6 cmH2O, the nurses started SBT trial: Continuos Positive Pressure Airways of 6cmH2O for at least 120 minutes and following discontinuation from ventilator.

Sponsors

ELENA PELI,MD
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. all patients that are clinically identified as prolonged to wean (failed 3 spontaneous breathing trials or 7 days or more of mechanical ventilation after the initial unsuccessful trial) and tracheostomized in ICU 2. improvement or resolution of the underlying causes of acute respiratory failure ratio between pressure partial artery of oxygen and fraction inspired oxygen (PaO2/FiO2) \>200 with fraction inspired oxygen (FiO2)\< 0,45. 3. pressure supported ventilation at the time of enrollment.

Exclusion criteria

1. patients assessed as easy weaning and not tracheostomized; 2. patients already tracheostomized on admission to ICU.

Design outcomes

Primary

MeasureTime frame
duration of weaningwithin the first 15 days (plus or minus 5 days) after start of weaning

Secondary

MeasureTime frame
duration of mechanical ventilationwithin the first 12 days (plus or minus 10 days) after start of mechanical ventilation

Other

MeasureTime frame
ICU length of staywithin the first 26 days (plus or minus 22 days) after ICU recovery
success of weaningspontaneous breathing for 48 hours

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026