Building Respiratory Support in East Africa Through High Flow Versus Standard Flow Oxygen Evaluation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBeth Israel Deaconess Medical Center

About this trial

Acute hypoxemia is common and deadly in resource variable settings. While studies in high income countries (HICs) have indicated a possible benefit to high flow oxygen as compared with standard flow oxygen, rigorous studies in low or lower middle income countries (LMICs) have not been performed. Studies in sepsis have demonstrated that interventions that improve outcomes in one context may actually be neutral or harmful in a different context.

The goal of this study is to test whether high flow oxygen results in better outcomes for hypoxemic adult patients, as compared with standard flow oxygen, in five LMIC hospitals. The main questions it aims to answer are:

1. For hypoxemic adults in these LMIC study settings, does high flow oxygen or standard flow oxygen result in lower mortality? 2. What are the facilitators and barriers to using high flow oxygen in these settings? 3. Does high flow or standard flow oxygen use more oxygen?

Participants will be randomized to receive either high flow oxygen through a large nasal cannula, or to receive standard flow oxygen, through nasal cannulas, face masks, or non-rebreather masks. Researchers will compare the outcomes for the two groups, to see if one group of patients has better outcomes than the other.

The study will also examine how much oxygen is used by the two patient groups, as well as other factors relevant to the feasibility of implementation of high flow oxygen in these sites.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age>=18 years AND

admitted to a study site hospital within the 24 hours prior to screening AND

SpO2<90% at time of first assessment OR

receiving oxygen at time of first assessment

Disqualifiers

imminent death (high clinical suspicion of death within 24 hours of admission)

patient or caregiver refusal of study participation

history of chronic respiratory failure (SpO2<90% or oxygen dependence for at least three months)

anatomical factors precluding the use of nasal cannula

Trial design

Design model

Parallel

Treatments tested in this trial

  • High flow oxygen

    Device

    humidified and heated oxygen delivered at high flow rates via nasal cannula, with protocol to target SpO2 90-94%

  • Standard flow oxygen

    Other intervention

    oxygen delivered at standard flow rates via nasal cannula, facemask, or nonrebreather mask, with protocol to target SpO2 90-94%

Treatment groups

1,600 Participants
are divided into 2 treatment groups
Group A: High flow oxygenExperimental treatment 1 intervention
Group B: Standard flow oxygenActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

In-hospital mortality

Death between randomization and end of hospitalization

Time frame
Day 90

Secondary outcomes

1

90-day mortality

Death between randomization and 90 days

Time frame
Day 90
2

90-day functional status

Functional status 90 days after randomization, as measured by the World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)

Time frame
Day 90
3

Need for mechanical ventilation

Met criteria for need to escalate respiratory therapy to NIV or invasive ventilation, or escalated to NIV or mechanical ventilation

Time frame
Day 90
4

Days requiring oxygen

Days requiring oxygen from randomization to end of hospitalization

Time frame
Day 90

Other outcomes

1

Oxygen consumption

Total oxygen consumed during hospitalization

Time frame
Day 90
2

90-day hospital re-admission

Re-admission to the hospital after discharge and before 90 days

Time frame
90 days

Sponsors and contacts

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