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Study identifier: NCT03976180 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

High-flow Oxygen for Vaso-occlusive Pain Crisis

Condition: Sickle Cell Disease  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants350
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 ma…

This description comes directly from the study's public registry record.

Talk to the study team

Armand Mekontso, MD, PhD  ·  +33 (1) 49 81 23 94  ·  armand.dessap@aphp.fr

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Locations (1)

Henri MondorCréteil, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT03976180