Informations générales (source: ClinicalTrials.gov)

NCT03971136 En recrutement IDF
Evaluation of the Interest of Pulmonary Ultrasound in the Diagnosis and Early Detection of Acute Thoracic Syndrome in Hospitalized Children for Vaso-occlusive Sickle Cell Crisis: Multicenter Prospective Study (ECHO-STA)
Interventional
  • Drépanocytose
N/A
Centre Hospitalier Intercommunal Creteil (Voir sur ClinicalTrials)
avril 2019
juillet 2023
29 juin 2024
ATS (acute thoracic syndrome) refers to acute pulmonary involvement in a sickle cell patient. The diagnosis is based on the association of clinical signs (fever or respiratory symptoms) with a recent pulmonary infiltrate on the chest x-ray. The main objective of the study is to evaluate the place of the pulmonary ultrasound for the diagnosis of ATS, in comparison with frontal chest x-ray.
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Etablissements

Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HP - Hôpital Armand Trousseau-La Roche Guyon Guillaume Thouvenin, MD Recrutement non commencé Contact (sur clinicalTrials)
CHI DE CRETEIL Fouad MADHI, MD En recrutement IDF Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Hôpital Antoine Béclère - 92141 - Clamart - France Mélanie TAVEIRA, MD Recrutement non commencé Contact (sur clinicalTrials)
Hôpital Bicêtre - 94270 - Le Kremlin-Bicêtre - France Irina CRAIU, MD Recrutement non commencé Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

- Age: ≥12 months and <18 years

- Has a major sickle cell disease whatever the genotype

- Admission to hospital for a febrile vaso-occlusive crisis (VOC) or not

- Evolving at home for less than 48h

- Concomitant treatment with hydroxycarbamide / hydroxyurea possible

- Signed consent

- Patients affiliated to a French social security scheme



- Child presenting an acute thoracic syndrome (ATS) from the outset at the admission

- Child who presented an ATS in the month preceding the inclusion

- Child in regular transfusion program or child who has received a hematopoietic stem
cell transplant

- Child hospitalized at least 5 times for VOC in the year preceding inclusion (psychic
problems making difficult the evaluation of the pain)

- Child who has already been included in the study during a previous VOC (each child
participates in the study only once)

- VOC evolving for more than 48 hours before admission to the emergency room

- Acute splenic sequestration crisis at admission