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Comparison of the Impact of Three Programs of Inspiratory Muscles. (PREDRIC)

Primary Purpose

Weaning From Mechanical Ventilation

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Martin
Cader
EDRIC
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Weaning From Mechanical Ventilation focused on measuring inspiratory muscles training programs, Ventilator-induced diaphragmatic dysfunction, Weaning, Intensive care unit

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient ventilated more than 18h in a controlled mode;
  • First single breathe trial of 2 hours failure;
  • Presence of sevrability criterias definied by the European consensus conference in 2007 an usually used:

    • diminution of the sedfative agents,
    • Patients with spontaneous beath in VAC mode or patient ventilated in a VSAI-PEP mode,
    • PaO2/FiO2 ≥150,
    • Absence d'inotropes ou de vasopresseurs à forte dose ou dose croissante (<1mg/h),
    • SaO2 > 90% with FiO2 ≤ 50%,
    • PEP ≤ 8cmH2O,
    • Corporal température between 36°C and 39°C,
    • Glasgow Score ≥ 8.

Exclusion Criteria:

  • Age < 18 years ;
  • medically unstable;
  • Poor vital pronostic at very short term;
  • Cardiac arrest with a poor neurological prognostic;
  • Neuromuscular disease ;
  • Pneumothorax non drained ;
  • Tracheostomy ;
  • Current pregnancy ;
  • Patients with guardianship or trusteeship.

Sites / Locations

  • Réanimation Médicale
  • Réanimation Médicale

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Experimental

Arm Label

Martin

Cader

EDRIC

Arm Description

A threshold-based IMT is performed like used by Martin in a randomized trial in 2011, in a view of inspiratory strength increase.

A threshold-based IMT is performed like used by Cader in a randomized trial in 2012, in a view of inspiratory endurance increase.

A new threshold-based IMT is performed, in a view of both inspiratory strength and endurance increase.

Outcomes

Primary Outcome Measures

Maximal Inspiratory Pressure score (inspiratory muscle strength index) performed by an external electronic device connected with a unidirectional valve.

Secondary Outcome Measures

Peak Pressure (inspiratory muscle endurance index) performed by an incremental threshold test.
Duration of the weaning period
ICU lengh of stay
Weaning success
Adverse events

Full Information

First Posted
July 28, 2016
Last Updated
May 12, 2020
Sponsor
University Hospital, Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT02855619
Brief Title
Comparison of the Impact of Three Programs of Inspiratory Muscles.
Acronym
PREDRIC
Official Title
Comparison of the Incidence of 3 Inspiratory Muscle Training Programs on Inspiratory Strength, on Difficult to Wean Patients in Intensive Care Unit: a Multi-centre Randomised Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
October 15, 2016 (Actual)
Primary Completion Date
February 22, 2020 (Actual)
Study Completion Date
March 22, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Ventilator-induced diaphragmatic dysfunction appears to contribute to slow weaning from mechanical ventilation. Several trials of inspiratory muscle training to facilitate weaning in intensive care have been performed, with inconsistent results, utilizing different methods of IMT in different populations. In this study, the investigators want to compare the incidence of 3 inspiratory muscle training programs on inspiratory strength, on difficult to wean patients in intensive care unit. This is a multi-center randomized trial not blinded with 3 parallels groups: Martin's group: a threshold-based IMT is performed like used by Martin in a randomized trial in 2011, in a view of inspiratory strength increase. Cader's group: a threshold-based IMT is performed like used by Cader in a randomized trial in 2010 , in a view of inspiratory endurance increase. EDRIC's group: a new treshold-based IMT is performed, in a view of both inspiratory strength and endurance increase. The investigators think that a new threshold-based IMT performed in a view of both inspiratory strength and endurance increase, is more effective and well tolerated than the 2 others protocols.
Detailed Description
The main objective of this study is to determinate which IMT program is the most effective on the inspiratory muscle strength and endurance increase. The investigators will be able to study the impact on the weaning time of IMT performed with the best protocol. The investigators are going to conduct a randomized trial with intention-to-treat analysis. Following 18h of invasive mechanical ventilation in a controlled mode, the failure of the first single breathe trial of 2 hours and the presence of sevrability criterias defined by the European consensus conference in 2007, 88 participants will be included. Participants will be randomizesd to receive one of the 3 protocols of IMT, 2 times per day, 7 days per week, from the inclusion to the extubation. The ratio of randomization will be 1:1:2 for a better evaluation of EDRIC's group wich propose a new IMT protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weaning From Mechanical Ventilation
Keywords
inspiratory muscles training programs, Ventilator-induced diaphragmatic dysfunction, Weaning, Intensive care unit

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Martin
Arm Type
Active Comparator
Arm Description
A threshold-based IMT is performed like used by Martin in a randomized trial in 2011, in a view of inspiratory strength increase.
Arm Title
Cader
Arm Type
Active Comparator
Arm Description
A threshold-based IMT is performed like used by Cader in a randomized trial in 2012, in a view of inspiratory endurance increase.
Arm Title
EDRIC
Arm Type
Experimental
Arm Description
A new threshold-based IMT is performed, in a view of both inspiratory strength and endurance increase.
Intervention Type
Procedure
Intervention Name(s)
Martin
Intervention Description
The physiotherapist perform the IMT using the threshold IMT inspiratory muscle trainer, connected to the intubation tube. He manage the resistance to the higher resistance tolerated by the patient in a set of 6 breaths. Participant repeats 4 sets of 6-10 breaths with 2 minutes of resting with mechanical ventilation between each set. This treatment is made twice a day, 7days per week from inclusion to extubation exept if Glasgow score is under 8, hyperthermia more than 39°c, haemodynamic's instability, or hypoxemia( PaO2/FiO2<150).
Intervention Type
Procedure
Intervention Name(s)
Cader
Intervention Description
The physiotherapist perform the IMT using the threshold IMT inspiratory muscle trainer, connected to the intubation tube. He manage the resistance to 30% of the Maximal Inspiratory Pressure initially recorded the day of the inclusion. Participant breaths against this resistance during 5 minutes. The resistance is daily increased of 10 % to the higher tolerated. This treatment is made twice a day, 7days per week from inclusion to extubation exept if Glasgow score is under 8, hyperthermia more than 39°c, haemodynamic's instability, or hypoxemia( PaO2/FiO2<150).
Intervention Type
Procedure
Intervention Name(s)
EDRIC
Intervention Description
The physiotherapist perform the IMT using the threshold IMT inspiratory muscle trainer, connected to the intubation tube. He manage the resistance at 30% of the Maximal Inspiratory Pressure of the day for the first set of 20 breaths with a resistance 's increasment of 10% at each set. Participant repeats 4 sets of 20 breaths with 2 minutes of resting with mechanical ventilation between each set. This treatment is made twice a day, 7days per week from inclusion to extubation exept if Glasgow score is under 8, hyperthermia more than 39°c, haemodynamic's instability, or hypoxemia( PaO2/FiO2<150).
Primary Outcome Measure Information:
Title
Maximal Inspiratory Pressure score (inspiratory muscle strength index) performed by an external electronic device connected with a unidirectional valve.
Time Frame
Baseline and up to day 25
Secondary Outcome Measure Information:
Title
Peak Pressure (inspiratory muscle endurance index) performed by an incremental threshold test.
Time Frame
Baseline and up to day 25
Title
Duration of the weaning period
Time Frame
up to day 25
Title
ICU lengh of stay
Time Frame
Day 30
Title
Weaning success
Time Frame
up to day 27
Title
Adverse events
Time Frame
Day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient ventilated more than 18h in a controlled mode; First single breathe trial of 2 hours failure; Presence of sevrability criterias definied by the European consensus conference in 2007 an usually used: diminution of the sedfative agents, Patients with spontaneous beath in VAC mode or patient ventilated in a VSAI-PEP mode, PaO2/FiO2 ≥150, Absence d'inotropes ou de vasopresseurs à forte dose ou dose croissante (<1mg/h), SaO2 > 90% with FiO2 ≤ 50%, PEP ≤ 8cmH2O, Corporal température between 36°C and 39°C, Glasgow Score ≥ 8. Exclusion Criteria: Age < 18 years ; medically unstable; Poor vital pronostic at very short term; Cardiac arrest with a poor neurological prognostic; Neuromuscular disease ; Pneumothorax non drained ; Tracheostomy ; Current pregnancy ; Patients with guardianship or trusteeship.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Perez, Professor
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Study Chair
Facility Information:
Facility Name
Réanimation Médicale
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
Réanimation Médicale
City
Lyon
ZIP/Postal Code
69004
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Comparison of the Impact of Three Programs of Inspiratory Muscles.

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