Outcomes of Vaso-occlusive Crisis in Pediatric Sickle Cell Disease

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-18
SponsorAssiut University

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • No intervention

    Other intervention

    retrospective 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

25 Participants
are divided into 1 treatment group
Group A: Sickle Cell pediatric patients1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Retrospective review of medical records from 2019 to 2024

Secondary outcomes

1

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.

Time frame
Throughout the study period (2019-2024)

Other outcomes

Sponsors and contacts

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