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NCT Number: NCT07782489

Pleuropulmonary Ultrasound Imaging in Patients With Sickle Cell Disease in a Vaso-occlusive Crisis. "ECHODREP"

Introduction Sickle cell disease is the most common inherited genetic disorder in France and worldwide. Its main acute manifestation is vaso-occlusive crisis, a frequent reason for emergency department visits. Acute chest syndrome is the leading complication and cause of death during vaso-occlusive crisis, occurring in approximately 15-20% of hospitalized episodes, often within the first few days after symptom onset. Early identification of patients at risk of developing acute chest syndrome remains a major clinical challenge. Although predictive clinical and biological scores exist, their ability to identify high-risk patients remains limited in daily practice. Chest X-ray has traditionally been used to support the diagnosis of acute chest syndrome, but its diagnostic performance and repeated radiation exposure are increasingly questioned. Lung ultrasound is a non-invasive bedside imaging tool that has shown good performance for detecting pleural effusion, alveolar consolidation and interstitial syndrome, and is increasingly used by emergency physicians. However, its diagnostic performance when systematically performed by emergency physicians in adult sickle cell patients presenting with vaso-occlusive crisis has not yet been specifically assessed.

Hypothesis / Objective We hypothesize that systematic pleuropulmonary ultrasound performed early after emergency department admission may help identify patients with vaso-occlusive crisis who are at risk of developing acute chest syndrome, and may allow earlier diagnostic assessment. The primary objective of the ECHODREP study is to evaluate the diagnostic performance of systematic pleuropulmonary ultrasound, performed by an emergency physician within six hours of admission, for the diagnosis of acute chest syndrome during hospitalization in adult sickle cell patients presenting with vaso-occlusive crisis.

Secondary objectives are to assess the association between ultrasound findings and the final diagnosis of acute chest syndrome, to describe patient outcomes according to ultrasound results, including hospitalization, admission to intermediate care, emergency department revisits and mortality at day 3, day 7 and day 28, and to compare ultrasound performance according to the operator's level of experience.

Method ECHODREP is a prospective, observational, single-arm, monocentric diagnostic performance study conducted in the Emergency Department of Henri-Mondor University Hospital. The study will include 200 adult patients with sickle cell disease - SS, SC or S-beta-thalassemia - presenting to the emergency department for vaso-occlusive crisis. Patients with a diagnosis of acute chest syndrome already established on arrival, patients previously included in the study, protected adults, and patients refusing participation will not be included.

After informed consent, a pleuropulmonary ultrasound will be performed within six hours of emergency department admission by an emergency physician investigator who is not involved in the patient's clinical care. The examination will assess twelve predefined lung zones. In order to avoid influencing standard care and to preserve the objectivity of the study, ultrasound findings obtained for research purposes will not be communicated to the treating medical team and will not be used for diagnostic or therapeutic decisions.

Patients will receive standard care for vaso-occlusive crisis according to local practice. A telephone follow-up will be performed at day 28 to collect vital status, emergency department revisits, hospitalizations and any secondary diagnosis of acute chest syndrome. At the end of follow-up, an independent adjudication committee, blinded to the research ultrasound findings, will determine the final diagnosis: uncomplicated vaso-occlusive crisis or acute chest syndrome.

The primary endpoint will be the diagnosis of acute chest syndrome within seven days after emergency department admission or before hospital discharge, based on the medical record. Diagnostic performance will be assessed by calculating sensitivity, specificity, positive and negative predictive values, likelihood ratios and area under the ROC curve, with 95% confidence intervals. Additional analyses will compare outcomes according to ultrasound findings and operator experience.

Conclusion This exploratory study will provide original data on the diagnostic performance of early pleuropulmonary ultrasound performed by emergency physicians in adult sickle cell patients presenting with vaso-occlusive crisis. If ultrasound demonstrates adequate diagnostic accuracy, it could contribute to earlier identification of acute chest syndrome, improve risk stratification in the emergency department and help optimize the management pathway of these patients. By evaluating both diagnostic performance and patient outcomes, ECHODREP may support the integration of lung ultrasound into future diagnostic strategies for acute chest syndrome in sickle cell disease.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • • Age ≥ 18 years
  • Sickle cell disease: SS, SC, or S-beta-thalassemia
  • Presentation to the Emergency Department for vaso-occlusive crisis
  • Patient affiliated with a social security system, either as beneficiary or entitled person
  • Patient informed about the study and having agreed to sign a free and informed consent form to participate in the study

Exclusion criteria

  • • Diagnosis of acute chest syndrome already established upon arrival at the Emergency Department
  • Pleuropulmonary ultrasound showing no abnormality but not having explored all twelve areas of interest [Appendix 1]
  • Patient already included in the study during a previous Emergency Department visit
  • Patient under guardianship or curatorship
  • Refusal to participate in the research

Treatment and study plan

Pleuropulmonary ultrasound

Other

A systematic bedside pleuropulmonary ultrasound will be performed within 6 hours of emergency department admission in adult patients with sickle cell disease presenting with vaso-occlusive crisis. The examination will be performed by an emergency physician investigator who is not involved in the patient's clinical care and will assess 12 predefined lung zones for pleural effusion, pulmonary consolidation and/or interstitial abnormalities.

Ultrasound findings obtained as part of the study will not be communicated to the treating medical team and will not be used for diagnostic or therapeutic decisions. The examination is non-invasive, performed according to usual clinical ultrasound practice, and is expected to take less than 10 minutes.

Primary outcomes

  1. Diagnosis of acute chest syndrome

    Time frame: Within 7 days after the emergency department visit, or until hospital discharge, as applicable.

    Formulation of the diagnosis of acute chest syndrome within 7 days after the emergency department visit or, where applicable, until hospital discharge, based on the patient's medical record.

    The outcome will be considered present if the medical record explicitly mentions at least one of the following:

    Diagnosis of acute chest syndrome; or occurrence of a new pulmonary auscultation abnormality, such as crackles or tubular breath sounds; or occurrence of a new radiological infiltrate, either alveolar or interstitial, associated with chest pain and/or decreased breath sounds.

Secondary outcomes

  1. Time to diagnosis of acute chest syndrome

    Time frame: Within 7 days after the emergency department visit, or until hospital discharge, as applicable.

    Time interval, expressed in days, between arrival at the emergency department and formulation of the diagnosis of acute chest syndrome

  2. Intermediate care unit stay

    Time frame: From emergency department visit to hospital discharge.

    Number of stays in intermediate care units and duration of intermediate care unit stay, expressed in days.

  3. Thoracic imaging abnormalities

    Time frame: After inclusion and pleuropulmonary ultrasound corresponded to D0 (Day 0), patients will be followed until Day 7 (D7) during hospitalization or, if discharged earlier, will be contacted between Days 3 (D3) and Days 7 (D7) after discharge of hospital

    Presence of abnormalities on other thoracic imaging examinations, if performed as part of routine care, including chest X-ray or chest computed tomography. Abnormalities of interest include pulmonary consolidation and/or pleural effusion.

  4. Hospitalization outcomes

    Time frame: From admission to the emergency department corresponded to Day 1 (D1) until hospital discharge or Day 7 (D7), and until Day 28 (D28) after inclusion that corresponded to follow visit.

    Number of hospitalizations and duration of hospitalization, expressed in days.

  5. All-cause mortality

    Time frame: At Day 3, Day 7, and Day 28 after the emergency department visit.

    All-cause mortality.

  6. Emergency department revisit related to sickle cell disease

    Time frame: At Day 3, Day 7, and Day 28 after the emergency department visit.

    Reconsultation at the emergency department for a reason related to sickle cell disease.

  7. Operator experience

    Time frame: At the time of pleuropulmonary ultrasound performance.

    Level of experience of the physician performing the pleuropulmonary ultrasound, defined as the number of years between the date of completion of the first qualifying diploma - emergency medicine specialty diploma or any other diploma validating level 1 emergency clinical ultrasound - and the date of ultrasound performance.

Study contacts

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

Christian Kassasseya, Doctor

CONTACT

[email protected]

(+33)1.49.81.21.11

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Performance Analysis of a Pleuropulmonary Ultrasound in the Emergency Department for Adult Patients With Sickle Cell Disease Undergoing an Vaso-occlusive Crisis

Acronym: ECHODREP

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 24, 2026
Registry last updated
Aug 24, 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.

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