Optiflow in Sequential Non-Invasive Ventilation

NCT02389166 | Completed DMC

• 1 other identifier: CHUBX 2013/28
• Study Type: interventional
• Target: 95
• Locations: 1 country
• Sites: 8

Brief Summary

Background : Patient with hypoxemic respiratory failure treated with NIV receive between NIV session oxygen therapy. Gaz exchange disorder with a decrease of the ratio between Partial Pressure of Arterial Oxygen (PaO2) and Inspired Fraction of Oxygen (FIO2) are noticed when NIV is stopped at the end of the session du to alveolar derecruitment Optiflow is a high flow oxygen delivery system used a heated humidifier and heated breathing circuit. In observational studies, Optiflow increase oxygenation of patients with hypoxemic respiratory failure. Oxygenation is better than under high-concentration mask and work of breathing is reduced. The aim of the study is to compare in acute hypoxemic respiratory failure, optiflow to oxygen therapy under high-concentration mask, on patients oxygenation between NIV sessions (measured as the difference between PaO2/FiO2 ratio at the beginning and at the end of the session), during the first two NIV sessions Study design : Prospective, randomized, controlled, multicentric, open clinical trial with two groups:

• control group with conventional clinical management, oxygen therapy and sequential used of NIV
• Optiflow group with high flow oxygen delivery system, conventional clinical management and sequential used of NIV for a period of 36 hours at least. Number of subjects: 100 (50 patients per group) patients admitted in intensive Care Unit for hypoxemic respiratory failure.

Conditions

Respiratory Failure

Outcome Measures

Primary Outcomes (1)

• Average of oxygenation differences measured as the delta between PaO2/FiO2ratio at the end of the first ans second NIV session and at the end of the first and second oxygen therapy session.

  Average of oxygenation differences measured as the delta between PaO2/FiO2 ratio at the end of the first NIV session and at the end of the first oxygen therapy session (according group of treatment) on the one hand and on the other hand the delta between PaO2/FiO2 ratio at the end of the second NIV session and at the end of the second oxygen thrapy session Five measurements of PaO2/FiO2 ratio are realized with arterial blood gases: * at the time of inclusion, * at the time of the end of first NIV session, * at the time of the end of first oxygen therapy session, or at the time of rescue NIV or at the time of réintubation * at the time of the end of second NIV session, * at the time of the end of second oxygen therapy session These five measurements are usually realised, and they are important to optimize patient management. The primary endpoint is based on these five measurements.

  28 days

Secondary Outcomes (9)

• comfort score dyspnea beetween the two NIV sessions

  28 days

• Incidence of serious adverse events between the two NIV sessions

  28 days

• Respiratory rate between the two NIV sessions

  28 days

• incidence of intubation during the NIV treatment of Acute respiratory distress syndrome (ARDS)

  28 days

• ICU mortality

  28 days

Study Arms (2)

Optiflow group

EXPERIMENTAL

Device: Optiflow

Control group

ACTIVE COMPARATOR

Device: Conventional oxygen therapy

Interventions

Optiflow DEVICE

Patients receive high flow oxygen delivery system, Optiflow, conventional clinical management and sequential used of NIV for a period of 36 hours at least. High flow oxygen nasal therapy (Optiflow) : The flow will be set at 40l/min to 60l/min The inspired fraction of oxygen (FiO2) is the same as that defined at the end of VNI session and may be adjusted in order to obtain a SaO2 between 94% and 98%.

Optiflow group

Conventional oxygen therapy DEVICE

Patients receive conventional oxygen therapy with high concentration mask, conventional clinical management, and sequential use of NIV Conventional oxygen therapy: The inspired fraction of oxygen (FiO2) is the same as that defined at the end of VNI session and may be adjusted in order to obtain a Arterial Oxygen Saturation (SaO2) between 94% and 98%.

Control group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patient at least 18 years old
• Patients affiliated to or benefiting of the French social welfare system
• Patients with ARDS on previously healthy lung. Acute respiratory insufficiency, defined as the PaO2/FIO2 ratio less than 200 mm Hg associated with the presence of lung infiltrates on chest radiograph
• Free and informed consent of patient
• Hospitalized in one of involved ICU

You may not qualify if:

• Existence of criteria for intubation.
• Refusal to participate in the study.
• Pregnancy
• Patient under guardianship or trusteeship
• Patients for whom a decision of non intubation has been decided.
• Patients who have received one or several NIV session for ARDS before hospital admission
• Home noninvasive ventilation
• Tracheostomy
• Hemodynamic instability
• Hypercapnia (PaCO2\>45 mm Hg).
• left ventricular failure (cardiogenic pulmonary acute edema).
• Ineffective coughing.
• Recent gastric or oesophageal surgery
• Severe ventricular rhythm disorder
• High digestive haemorrhage

Sponsors & Collaborators

• University Hospital, Bordeaux: lead

Study Sites (8)

Service de réanimation - CH de la côte basque

Bayonne, Aquitaine, 64100, France

Location

Service de réanimation médicale - CHU de Bordeaux

Bordeaux, Aquitaine, 33000, France

Location

Service de Réanimation Polyvalente - CH de Libourne

Libourne, Aquitaine, 33505, France

Location

Service de Réanimation - CH de Perigueux

Périgueux, Aquitiane, 24000, France

Location

Service de Réanimation Polyvalente - CHU de Toulouse

Toulouse, Midi-pyrenees, 31059, France

Location

Service de Réanimation Polyvalente - CH d'Agen

Agen, 47923, France

Location

Réanimation polyvalente - CH d'Albi

Albi, 81000, France

Location

Réanimation Polyvalente - CH de Mont de Marsan

Mont-de-Marsan, 40024, France

Location

MeSH Terms

Conditions

Respiratory Insufficiency

Condition Hierarchy (Ancestors)

Respiration Disorders; Respiratory Tract Diseases

Study Officials

• Antoine BENARD, Docotor

  University Hospital, Bordeaux

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 3, 2015
• First Posted: March 17, 2015
• Study Start: June 25, 2015
• Primary Completion: February 5, 2019
• Study Completion: March 5, 2019
• Last Updated: July 31, 2019

Record last verified: 2019-07

Data Sharing

• IPD Sharing: Will not share

Locations

FR (8)