Actively Recruiting
High-flow Oxygen for Vaso-occlusive Pain Crisis
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-07-28
350
Participants Needed
1
Research Sites
291 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
F
Fisher and Paykel Healthcare
Collaborating Sponsor
AI-Summary
What this Trial Is About
Sickle cell disease (SCD) is characterized by recurrent vaso-occlusive pain crisis (VOC), which may evolve to acute chest syndrome (ACS), the most common cause of death among adult patients with SCD. Currently, there is no safe and effective treatment to abort VOC or prevent secondary ACS. Management of VOC mostly involve a symptomatic approach including hydration, analgesics, transfusion, and incentive spirometry, which was investigated in a very limited number of patients (\<30). The polymerisation of HbS is one major feature in the pathogenesis of vaso-occlusion. Among factors determining the rate and extent of HbS polymer formation, the hypoxic stimulus is one of the most potent and readily alterable. Current guidelines recommend oxygen therapy in patients with VOC in order to maintain a target oxygen saturation of 95%. Low-flow nasal oxygen (LFNO) is routinely used to achieve this normoxia approach, particularly in patients at risk of secondary ACS because they may experience acute desaturation. In contrast, various case series suggest a potential beneficial role of intensified oxygen therapy targeting hyperoxia for the management of VOC, particularly with the use of hyperbaric oxygen, but the latter is difficult to implement in routine clinical practice. A recent high-flow nasal oxygen (HFNO) technology allows the delivery of humidified gas at high fraction of inspired oxygen (FiO2) through nasal cannula. The FiO2 can be adjusted up to 100% (allowing hyperoxia that may reverse sickling) and the flow can be increased up to 60 L/min (which generates positive airway pressure and dead space flushing, that may prevent evolution of VOC towards ACS by alleviating atelectasis and opioid-induced hypercapnia). In patients with acute respiratory failure, HFNO has been shown to improve patient's comfort, oxygenation, and survival as compared to standard oxygen or non-invasive ventilation. The aim of the present study is to test the efficacy and safety of HFNO for the management of VOC and prevention of secondary ACS. The investigators will use a multi-arm multi-stage (MAMS) design to achieve these goals. HFNO will be delivered through AIRVO 2 (Fisher and Paykel Healthcare, New Zealand), a device that incorporates a turbine allowing its use in hospital wards.
CONDITIONS
Official Title
High-flow Oxygen for Vaso-occlusive Pain Crisis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis of major sickle cell disease syndrome (SS, SC, Sβ0, or Sβ+)
- Experiencing a vaso-occlusive crisis defined by acute pain requiring opioids, affecting at least one body part, not caused by other reasons
- Intermediate-to-high risk for secondary acute chest syndrome based on reticulocyte count or specific blood and imaging criteria
- Able to give informed consent
- Affiliated with social security
You will not qualify if you...
- Presence of primary acute chest syndrome at the time of randomization
- Need for parenteral opioids for more than 72 hours before inclusion
- Known pregnancy or current breastfeeding
- Known cerebral vasculopathy or history of stroke due to Moya Moya or major vessel stenosis/occlusion
- Known ischemic heart disease or typical chest angina
- Currently enrolled in another investigational drug study
- Legal incapacity
- Prisoners or involuntarily incarcerated individuals
- Anatomical reasons preventing nasal cannula placement
AI-Screening
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Trial Site Locations
Total: 1 location
1
Henri Mondor
Créteil, France, 94000
Actively Recruiting
Research Team
A
Armand Mekontso, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
4
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