Comparison of Two Ventilator Mode During the Night: New Strategy of Mechanical Ventilation Weaning

NCT ID: NCT01573481

Last Updated: 2025-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-31

Study Completion Date

2015-01-31

Brief Summary

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The purpose of the study is to compare pressure controlled continuous mandatory ventilation versus pressure support ventilation during the night for weaning to mechanical ventilation in chronic obstructive pulmonary disease patients and their impact onto sleep quality.

Detailed Description

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Conditions

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Weaning Failure COPD Exacerbation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Pressure support ventilation

Patients in this group are ventilated during the night (10 PM to 9 AM) with pressure support ventilation mode. The level of the pressure support is the same as the previous day.

During the day (9 AM to 10 PM), patients are ventilated with pressure support ventilation (the level of pressure support is progressively decreased).

Group Type ACTIVE_COMPARATOR

pressure support ventilation

Intervention Type OTHER

Patients in this group are ventilated during the night with pressure support ventilation mode. The level of the pressure support is the same as the previous day.

Pressure controlled ventilation

Patients in this group are ventilated during the night (10 PM to 9 AM) with pressure controlled ventilation mode. The level of inspiratory pressure is set to 20 cm H2O and the respiratory rate is adjusted to avoid any spontaneous breathing (respiratory rate \> or equal to 12 breath per min). During the day (9 AM to 10 PM), patients are ventilated with pressure support ventilation (the level of pressure support is progressively decreased).

Group Type ACTIVE_COMPARATOR

Pressure controlled ventilation

Intervention Type OTHER

Patients in this group are ventilated during the night (10 PM to 9 AM) with pressure controlled ventilation mode. The level of inspiratory pressure is set to 20 cm H2O and the respiratory rate is adjusted to avoid any spontaneous breathing (respiratory rate \> or equal to 12 breath per min).

Interventions

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pressure support ventilation

Patients in this group are ventilated during the night with pressure support ventilation mode. The level of the pressure support is the same as the previous day.

Intervention Type OTHER

Pressure controlled ventilation

Patients in this group are ventilated during the night (10 PM to 9 AM) with pressure controlled ventilation mode. The level of inspiratory pressure is set to 20 cm H2O and the respiratory rate is adjusted to avoid any spontaneous breathing (respiratory rate \> or equal to 12 breath per min).

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The patient and/or legal representative of the patient has provided a written informed consent before inclusion in the study
* The patients is hospitalized in respiratory and critical care unit (university hospital of AMIENS, FRANCE)
* the patient is mechanically ventilated (ventilator model : puritan-bennett B840)
* Pulmonary disease,chronic obstructive (Spirometry and Blood Gas Analysis in chronic state before admission)
* stable cardiovascular status (cardiac frequency \< 140 beats/min and systolic blood pressure : 90-160 mmHg without catecholamines)
* midazolam \< 0,05mg/kg/h
* sufentanyl \< 0,05µ/kg/h
* the disorder that caused respiratory failure and prompted mechanical ventilation is treated
* the clinician suspects the patient may be ready to begin the weaning process
* inspiratory oxygen fraction (FiO2) \< 50%
* positive end-expiratory pressure \< or equal 8cmH2O
* during the day, the patient tolerate pressure support ventilation (pressure support level \< 15cmH2O
* respiratory frequency (FR) \< 35 breaths/min
* tidal volume (VT) \> 5ml/kg
* PaO2/FiO2 \> 200 mmHg
* FR/VT \< 105 breaths/min/L

Exclusion Criteria

* sleep apnea, central
* narcolepsy
* Encephalopathy, Metabolic AND Encephalitis
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire, Amiens

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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ANDREJAK Claire, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Amiens

JOUNIEAUX Vincent, MD PhD

Role: STUDY_DIRECTOR

CHU Amiens

BASILLE Damien, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Amiens

ROGER Pierre-Alexandre, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Amiens

ROSE Dominique, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Amiens

MONCONDUIT Julien, MD

Role: PRINCIPAL_INVESTIGATOR

CHU Amiens

Locations

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Pneumologie et Réanimation Respiratoire

Amiens, , France

Site Status

Countries

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France

References

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Other Identifiers

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PI2012_843_0016

Identifier Type: -

Identifier Source: org_study_id

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