Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07703566

CPAP for Hypoxemic Acute Chest Syndrome in Sickle Cell Disease

Sickle cell disease (SCD) is a severe hemoglobinopathy, considered the first monogenic disease in the world. Acute chest syndrome (ACS), one of the most frequent and serious complications of SCD, is defined by the association of fever and/or acute respiratory symptoms with a new pulmonary infiltrate on chest imaging. ACS is characterized by lung consolidation, severe pulmonary vascular dysfunction, with potential role for regional alveolar hypoxia. Therefore, improving alveolar oxygenation and limiting lung consolidation are key objectives of the treatment of ACS, in addition to ensuring pain relief and giving blood transfusions and antibiotics. Bilevel non-invasive ventilation failed in improving outcomes during ACS (Fartoukh 2010). These results are in accordance with those reported in other forms of acute lung injury (Frat 2015), with conflicting results. Among other explanations, NIV may favour high tidal volume ventilation leading to patient self-inflicted lung injury (P-SILI) (Carteaux 2016). Continuous positive airway pressure (CPAP) is a simple to use and affordable technique for non-invasive ventilatory support, that theoretically exposes to a lower risk of P-SILI (Carteaux 2021). In patients with acute hypoxemic respiratory failure (AHRF), applying a positive pressure to the airway opening has been shown to mitigate the reduction in functional residual capacity and to improve respiratory mechanics and gas exchange. In a randomized controlled trial (RCT) conducted in patients with AHRF, CPAP achieved early physiologic improvement (Delclaux 2000). Recent results also suggest that CPAP reduces the composite outcome of intubation or death in adults with AHRF due to COVID-19 in a large multicentre study (RECOVERY-R) (Perkins 2022). In addition, CPAP can be safely used at early stages in the wards, with a frugal approach, using virtual valves (Carteaux 2021). In patients with SCD, CPAP has shown benefits when used at night in children with sleep apnea (Marshall 2009), or for the peri-operative management (Leff 2007). CPAP is also used in clinical practice for hypoxemic ACS (Heilbronner 2021), but it has not been formally assessed in this setting.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • SCD patient of all genotypes (SS, SC, S/β0 and S/β+)
  • Age ≥ 18 years old
  • Hospitalised for ACS (defined as the association of fever and/or acute respiratory symptoms with a new pulmonary infiltrate on chest imaging)
  • Requiring supplemental O2 ≥ 2 L/min for SpO2 ≥ 95%
  • Informed consent from the patient
  • Affiliated to a social security regime

Exclusion criteria

  • Patient having both ACS criteria and need for supplemental O2 ≥ 2 L/min for SpO2 ≥ 95% since more than 48 hours
  • Requirement for home supplemental O2 or home CPAP / NIV.
  • Signs of worsening respiratory failure mandating intubation (as defined in (Helms et al., 2024))
  • Current enrolment in another interventional research concerning a respiratory support during ACS
  • Known legal incapacity (patients under guardianship or curatorship)
  • Exacerbation of asthma, chronic obstructive pulmonary disease or another known or suspected chronic respiratory disease
  • Absolute contraindications to CPAP, including any of the following: patient not cooperating or opposing the technique, pneumothorax not drained, chest wound blowing, uncontrollable vomiting, upper gastrointestinal bleeding, craniofacial trauma, severe upper airway obstruction, traumatic tetraplegia at the initial phase, cardiac arrest, shock (need for vasopressor), or Coma Glasgow scale <12.
  • Known pregnancy, breast feeding, women with childbearing potential will be tested for pregnancy and excluded if pregnant,

Treatment and study plan

O2+CPAP group

Other

ACS episodes assigned to this group will receive supplemental O2 in addition to periods of CPAP. CPAP will target a positive pressure between 5 and 10 cmH2O. CPAP will be given discontinuously (≥6 hours/day) based on patient tolerance . CPAP sessions will be stopped when the patient achieves the criteria for cessation of supplemental O2. These criteria will be the same as in the O2 group. No sedation will be used for CPAP tolerance.

Primary outcomes

  1. Time to résolution of acute chest syndrome (ACS)

    Time frame: Up to randomization

    time to resolution of ACS, defined as the time from randomization to the joint resolution of fever (body temperature < 38°C), chest pain (visual analog scale, VAS ≤ 3 cm, morphine ≤ 40mg/24h), dyspnea (VAS ≤ 3 cm, respiratory rate < 25/min, no ventilatory support), and hypoxemia (SpO2 > 92% on room air) (Mekontso Dessap, Habibi, et al., 2025).

    If a VAS is unavailable, a verbal rating scale will be used. Resolution of ACS will be assessed every 8 to 12 hours and will be considered achieved if sustained across 2 to 3 consecutive evaluations (i.e., over a 24-hour period).

Secondary outcomes

  1. Mortality

    Time frame: up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation.

    All-cause mortality

  2. Length of hospital stay

    Time frame: up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation.

  3. Length of ICU stay

    Time frame: up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation.

  4. Need for catecholamine infusion

    Time frame: From randomisation to discharge or Day-28

    dobutamine, dopamine, adrenaline or noradrenaline

  5. Number of red blood cell units transfused

    Time frame: From randomisation to discharge or Day-28

  6. Volume of blood exsanguination

    Time frame: From randomisation to discharge or Day-28

  7. Need for invasive ventilation

    Time frame: From randomisation to discharge or Day-28

  8. Number of days free from any respiratory support

    Time frame: From randomisation to discharge or Day-28

  9. Need for antibiotics therapy

    Time frame: From randomisation to discharge or Day-28

  10. Change in arterial blood gases (PaO2/FiO2 ratio), routine laboratory markers (lacticodeshydrogenase), and chest imaging (X-ray or lung ultrasound score)

    Time frame: within 3 days post-randomisation

  11. Readmissions for VOC

    Time frame: up to 3 months

  12. Readmissions for ACS

    Time frame: up to 3 months

  13. Quality of life questionary

    Time frame: At inclusion, Day-28, and 3 months

    EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L) Index score. The index score ranges from less than 0 (health states considered worse than death; country-specific minimum) to 1.0 (full health). Higher scores indicate better health-related quality of life.tatus and monitor changes over time.

Study contacts

Contact information is provided by the study sponsor or research team.

Armand MEKONTSO-DESSAP

CONTACT

[email protected]

Samia BALOUL

CONTACT

[email protected]

01 49 81 33 85

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Continuous Positive Airway Pressure for Hypoxemic Acute Chest Syndrome in Patients With Sickle Cell Disease

Acronym: SIPAP

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jul 14, 2026
Registry last updated
Jul 23, 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.

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