About this trial
This study aims to assess the incidence and clinical outcomes of vaso-occlusive crises in pediatric patients with sickle cell disease. Data will be collected and analyzed to identify risk factors and related complications.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Children aged 1-18 years. Confirmed diagnosis of sickle cell anemia by hemoglobin electrophoresis or high-performance liquid chromatography .
Disqualifiers
Patients with other hemoglobinopathies (e.g., thalassemia). Patients with incomplete medical records. Children with coexisting chronic diseases that may confound pain crises .
Trial population
Pediatric patients (1-18 years) with confirmed Sickle Cell Disease. The study observes the incidence and outcomes of vaso-occlusive crises (VOCs). Both sexes are eligible. Healthy volunteers are not included.
Trial design
Cohort
Retrospective
Treatments tested in this trial
No intervention
Other interventionretrospective observational study. No intervention will be administered; data will be collected from existing medical records of pediatric sickle cell patients at Assiut University Hospital.
Treatment groups
Trial outcomes
Primary outcomes
Incidence of vaso-occlusive crisis in pediatric sickle cell patients
Frequency of vaso-occlusive crisis episodes will be identified through retrospective chart review of pediatric sickle cell patients.
Secondary outcomes
Complications associated with vaso-occlusive crisis (e.g., acute chest syndrome, stroke, infections)
Complications related to vaso-occlusive crisis will be identified and documented from patient records.
Sponsors and contacts
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