Skip to main content
OpenTrials
Completed

NCT Number: NCT02389166

Optiflow in Sequential Non-Invasive Ventilation

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Respiratory Failure Respiration Disorders Respiratory Insufficiency Respiratory Tract Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Service de réanimation - CH de la côte basque, Bayonne, Aquitaine, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 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

Exclusion criteria

  • 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
  • Lack of collaboration
  • Pernicious vomiting
  • Upper airway obstruction
  • Severe sepsis.
  • Undrained pneumothorax.

Treatment and study plan

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%.

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%.

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.

    Time frame: 28 days

    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.

Secondary outcomes

  1. comfort score dyspnea beetween the two NIV sessions

    Time frame: 28 days

    The comfort score and dyspnea will be assessed between the two NIV sessions

  2. Incidence of serious adverse events between the two NIV sessions

    Time frame: 28 days

  3. Respiratory rate between the two NIV sessions

    Time frame: 28 days

    Respiratory rate to assess work of breathing between the two NIV sessions

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

    Time frame: 28 days

  5. ICU mortality

    Time frame: 28 days

  6. 28 days survival

    Time frame: 28 days

  7. Hospital mortality

    Time frame: 28 days

  8. ICU length of stay

    Time frame: 28 days

  9. duration of mechanical ventilation

    Time frame: 28 days

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Registry information

Official study title

Randomized Clinical Trial Comparing High Flow Oxygen Delivery System (Optiflow) With Oxygen Therapy Under High-concentration Mask on Oxygenation of Patients Who Receive Sequential Non-Invasive Ventilation (NIV) Sessions

Acronym: VNI-HD

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Mar 17, 2015
Registry last updated
May 22, 2026

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.

Related clinical trials

Published trials that share one or more normalized conditions with this study.