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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03689309
Other study ID # CHRO-2018-06
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 16, 2018
Est. completion date July 15, 2020

Study information

Verified date July 2020
Source Centre Hospitalier Régional d'Orléans
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In intensive care unit (ICU), mechanical ventilation (MV) is part of routine care.

Weaning phase is a daily preoccupation for the caregivers. Prolonged MV can lead to many complications. Failing the weaning phase expose the patient to the need for reintubation, that improves the mortality.

The caregiver faces a major problem, in one hand the need to wean properly and quickly and on the other the risk of reintubation.

In order to help the clinician making the good choice, the spontaneous breathing trial (SBT) is a key tool. The international literature provides the investigators many ways to perform the SBT. The most common is the T-piece; the patient is disconnected from the ventilator and connected to a T-piece that can provide supplemental oxygen. Another one is the Support pressure trial, the patient is still connected to the ventilator, but the setups are changed to recreate the T-piece conditions.

In many French ICU's, the SBT is performed by using a heat humidifier filter that is directly connected to the endotracheal tube, this filter allows the clinician to provide supplemental oxygen in accordance with the patient need.

In high risk for reintubation patients, the SBT can create physical stress, that lead to prolonged MV.

In our ICU, for those patients, the investigators perform the SBT by connecting the patient to a device that provides high flow oxygen trough endotracheal connector for tracheotomy.

The investigators hypothesis that high flow oxygen SBT, will allow the high risk for reintubation patients to succeed the SBT.


Description:

The investigators proposed to compare 2 strategies for SBT in high risk for reintubation patients:

1. Classic SBT (C-SBT)

2. High Flow Oxygen SBT (HFO-SBT)

This prospective randomized study had 2 conjoint primary outcome:

1. The HFO-SBT shows a better actuarial rate for extubation at day 7 from the begin of the weaning phase

2. Compare the reintubation rate at D7 from the extubation


Recruitment information / eligibility

Status Completed
Enrollment 106
Est. completion date July 15, 2020
Est. primary completion date July 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18 yrs.

- Admission in ICU

- Mechanically ventilated > 24 hours

- Mechanically ventilated using support ventilation mode

- Patient with one of these criterion:

- Cardiac disease (left ventricular dysfunction LVEF <46%, antecedent of ischemic heart disease, antecedent of acute pulmonary edema)

- Respiratory disease (COPD, Emphysema, bronchectiasis, asthma, obesity-hypoventilation syndrome, restrictive pulmonary disease)

- Informed and signed consent from the patient or next of kin.

Exclusion Criteria:

- Head trauma as a cause for ICU admission

- Neuromuscular disease prior ICU admission

- Tracheotomized patient

- Pregnancy

- Decision not to forgo life sustaining therapy

- Patient not affiliated with a social security organism

- Adult private from his liberty with judicial decision

- Patient that have already been included in the study

Study Design


Intervention

Procedure:
High Flow Oxygen SBT
The patient is disconnected from the ventilator and remains 30 minutes without support but high flow oxygen delivered through a dedicated piece that is usually connected on tracheotomy.

Locations

Country Name City State
France CHR d'Orleans Orléans

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Régional d'Orléans

Country where clinical trial is conducted

France, 

References & Publications (3)

Brochard L, Rauss A, Benito S, Conti G, Mancebo J, Rekik N, Gasparetto A, Lemaire F. Comparison of three methods of gradual withdrawal from ventilatory support during weaning from mechanical ventilation. Am J Respir Crit Care Med. 1994 Oct;150(4):896-903. — View Citation

Ladeira MT, Vital FM, Andriolo RB, Andriolo BN, Atallah AN, Peccin MS. Pressure support versus T-tube for weaning from mechanical ventilation in adults. Cochrane Database Syst Rev. 2014 May 27;(5):CD006056. doi: 10.1002/14651858.CD006056.pub2. Review. — View Citation

Thille AW, Richard JC, Brochard L. The decision to extubate in the intensive care unit. Am J Respir Crit Care Med. 2013 Jun 15;187(12):1294-302. doi: 10.1164/rccm.201208-1523CI. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Actuarial rate of extubation This prospective randomized study had 2 conjoint primary outcomes to ensure the safety for the patients:
The HFO-SBT shows a better actuarial rate for extubation at day 7 from the begin of the weaning phase
Compare the reintubation rate at D7 from the extubation
This prospective randomized study had 2 conjoint primary outcomes to ensure the safety for the patients:
The HFO-SBT shows a better actuarial rate for extubation at day 7 from the begin of the weaning phase
Compare the reintubation rate at D7 from the extubation
Day 7
Primary Reintubation Rate This prospective randomized study had 2 conjoint primary outcomes to ensure the safety for the patients:
The HFO-SBT shows a better actuarial rate for extubation at day 7 from the begin of the weaning phase
Compare the reintubation rate at D7 from the extubation
Day 7
Secondary Success rate of the first SBT Success rate of the first SBT will be compared between the two groups. Day 0
Secondary Ventilator free-days Ventilator free-days at day 28 from the admission in ICU Day 28
Secondary Rate of Ventilator Associated Pneumonia Rate of Ventilator Associated Pneumonia at day 7 from the extubation Day 7
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