The Implementation of the Automated Erythrocytapheresis in Egyptian Sickle Cell Disease Center
NCT03903289 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2024-01-11
Summary
Improvements of health infrastructure, preventive care and clinical treatment have reduced the morbidity and mortality of sickle cell disease (SCD). However, SCD is still an increasing national health problem, with increase longevity the chronic effect of sustained hemolysis and episodic vaso-occlusive events and the recurrent episodes of ischemic reperfusion injury drive the development of progressive end organ complications and cardiovascular, pulmonary, neurological and renal systems are most commonly affected. Today there is hope for a cure using hematopoietic stem cell transplantation (HSCT). However, at present; the procedure is infrequently performed and very expensive. In this research we will assess the effect of implementation of the automated erythrocytapheresis in the outcome of sickle cell disease in single Egyptian center.
Conditions
Interventions
- PROCEDURE
-
Automated red cell exchange
Erythrocytapheresis is an automated red cell exchange procedure that removes blood that contains HbS from the patient while simultaneously replacing that same volume with packed red cells free of HbS.
- PROCEDURE
-
Manual red cell exchange
Active Comparator: Manual red cell exchange
- PROCEDURE
-
Simple red cell transfusion
Active Comparator: Simple red cell transfusion
Sponsors & Collaborators
-
Ain Shams University
lead OTHER
Principal Investigators
-
Fatma Solima SE Ebeid, MD · Faculty of Medicine, Ain Shams university
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 2 Years
- Max Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-08-16
- Primary Completion
- 2025-12-31
- Completion
- 2026-01-31
Countries
- Egypt
Study Locations
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