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Completed

NCT Number: NCT02620358

Two Opposite Strategies of Weaning From Mechanical Ventilation

This study compares two opposite strategies of weaning from Mechanical Ventilation. One of them is Low Pressure Support Ventilation during 30 minutes and the other is T-Tube for 2 hours. The aim of the study is to know witch one has a higher successful extubation rate.

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Key information

Conditions

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

The final stage of weaning from Mechanical Ventilation is known as Spontaneous Breathing Test (SBT). Some studies in the last 20 years have compared different strategies of weaning.

The SBT using T-Tube versus Low Pressure Support Ventilation (PSV) for 2 hours didn't show differences in successful extubation.

No difference in successful extubation rate were seen with the T-Tube for 30 or 120 minutes, or the Low PSV for 30 minutes or 2 hours For this reason the actual guidelines recommend to use T-Tube or Low PSV from 30 minutes to 2 hours with the same level of evidence.

Nevertheless, no studies have compared two opposite strategies like T-Tube for 2 hours (High work of breathing) versus Low PSV for only 30 minutes (Low work of breathing). Whereas the high work of breathing approach can be more specific for detecting more fitted patients, the low work of breathing method may reduce fatigue during SBT allowing more patients to be extubated.

We have designed a prospective, multicentric controlled and randomized study to compare this two opposite strategies of weaning: T-Tube for 120 minutes versus PSV 8 cmH2O for 30 minutes.

When patients show weaning criteria the randomly assigned SBT will be done.

We consider weaning criteria:

  • Adequate cough
  • Not too many respiratory secretions.
  • Primary pathology solved.
  • Clinical stability: Heart Rate (HR) < 140 bpm, Systolic Blood Pressure (SBP) 90-160 mmHg.
  • Correct oxygenation: SatO2 > 90% with FiO2 < 0,4.
  • Correct ventilatory pattern: Respiratory rate (RR) < 35 pm, Maximal Inspiratory Pressure (MIP) < -20 cmH2O, Tidal volume (TV) > 10 ml/kg, RR/TV < 100 pm/l.
  • Adequate level of consciousness

Patients who succeed SBT will be extubated. Patients who fail SBT will be reconnected to the ventilator in the previous modality. These patients won't be randomized in future SBT.

We consider SBT failure:

Subjective Index:

  • Neurological: Agitation or anxiety, Low level of consciousness.
  • Increased work of breathing: accessory muscle use, dyspnea.

Objective Index:

  • Hypoxemia: PaO2 < 60 mmHg or SatO2 < 90% with FiO2 > 50%.
  • Tachypnea: RR > 35 pm.
  • Hemodynamic instability: HR > 140 bpm, SBP > 180 mmHg, Arrhythmia.

Extubation failure will be registered within the first 72 hours after extubation.

We consider extubation failure:

  • Respiratory acidosis: pH < 7,32, PaCO2 > 45 mmHg.
  • Hypoxemia: SatO2 < 90% or PaO2 < 60 mmHg with FiO2 > 0,5.
  • Deteriorating level of consciousness, Glasgow Coma Scale < 13.
  • Uncontrolled agitation.
  • Signs of fatigue.

Treatment of extubation failure will be decided by the attending physician: Reintubation, High Flow Oxygen therapy or Non Invasive Ventilation.

Reintubated patients won't be randomized in future SBT.

An interim analysis will be done when half of the simple is recruited.

Successful extubation will be analyzed by Kaplan-Meier survivial curves and logistic multivariable analysis with confounding variables.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • More tan 18 years old
  • More tan 24 hour of Mechanical Ventilation ready for weaning

Exclusion criteria

  • Tracheostomy
  • Non reintubation orders

Treatment and study plan

T Tube for 120 minuts

Other

Spontaneous Breathing Trial using T Tube for 120 minutes.

Pressure Support Ventilation of 8 cmH2O for 30 minutes

Other

Spontaneous Breathing Trial using Pressure Support Ventilation of 8 cmH2O for 30 minutes

Primary outcomes

  1. Succesful extubation rate

    Time frame: 72 hours

    Rate of succesful extubation after one of the weaning strategy

Secondary outcomes

  1. ICU Length of Stay

    Time frame: 3 month

    Define the ICU Length os Stay of each group

  2. Hospital Length of Stay

    Time frame: 3 month

    Define the Hospital Length of Stay of each group

  3. Mortality

    Time frame: 3 month

    Definte mortality rate of each group

  4. Reintubation rate

    Time frame: 72 hours

    Rate of reintubation in each group the first 72 hours

Sponsors and collaborators

Lead sponsor

Althaia Xarxa Assistencial Universitària de Manresa

Other

Collaborators

  • Complejo Hospitalario Universitario de Badajoz
  • Complejo Hospitalario Universitario de Santiago
  • Complejo Hospitalario Universitario de Vigo
  • Complejo Hospitalario de Caceres
  • Complexo Hospitalario de Ourense
  • Consorci Sanitari de Terrassa
  • Hospital Clínico Universitario de Valencia
  • Hospital General Universitario Elche
  • Hospital General Universitario Gregorio Marañon
  • Hospital General Universitario Morales Meseguer
  • Hospital General Universitario de Alicante
  • Hospital Mutua de Terrassa
  • Hospital Universitari Joan XXIII de Tarragona.
  • Hospital Universitari de Bellvitge
  • Hospital Universitario Araba
  • Hospital Universitario Central de Asturias
  • Hospital Universitario Infanta Cristina
  • Hospital Universitario Marqués de Valdecilla
  • Hospital Universitario Reina Sofia de Cordoba
  • Hospital Universitario Rey Juan Carlos
  • Hospital Universitario de Canarias
  • Hospital de Granollers
  • Hospital de Henares
  • Hospital de Mataró
  • Hospital de Sabadell
  • Hospital de Sagunto
  • Hospital de Sant Joan Despí Moisès Broggi
  • Hospital de Toledo
  • Hospital del Mar
  • Hospital of Navarra

Registry information

Official study title

Two Opposite Strategies of Weaning From Mechanical Ventilation: High Work of Breathing Versus Low Work of Breathing

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 3, 2015
Registry last updated
Mar 31, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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