Red blood cell exchange in sickle cell
DeviceOne Red Blood Cell Exchange using Spectra Optia Apheresis System per enrolled patient
Other names: Specta Optia Apheresis System
NCT Number: NCT01736657
The purpose of this study is to evaluate the performance of the Spectra Optia system red blood cell exchange (RBCx) protocols (exchange and depletion/exchange) in study participants with sickle cell disease.
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Notify Me12 year and older
All sexes
Interventional
Not applicable
Children's of Alabama, Birmingham, Alabama, United States
Evaluate the performance of the Spectra Optia system red blood cell exchange (RBCx) protocols (exchange and depletion/exchange) in study participants with sickle cell disease. Open label design.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
One Red Blood Cell Exchange using Spectra Optia Apheresis System per enrolled patient
Other names: Specta Optia Apheresis System
Time frame: Length of the procedure
The primary endpoint evaluated the mean ratio of the Actual Fraction of Cells Remaining (FCRa: as measured by Post-Procedure % HbS) to the Predicted Fraction of Cells Remaining (FCRp: as predicted by the Spectra Optia system FCR algorithm multiplied by the Pre-Procedure % HbS), in the evaluable population (60 pts). The pre-defined range for the mean ratio of the FCRa to the FCRp was 0.75 to 1.25.
Time frame: Length of the procedure
The procedural success of the Spectra Optia System is defined as the ability of the device to complete a red blood cell exchange (RBCx) and to obtain a satisfactory exchange by lowering the patient's hemoglobin S, as determined by the investigator in the evaluable population (60 pts).
Time frame: Length of the procedure
Measurement of the patient post-procedure hematocrit compared to the final target hematocrit calculated by the Spectra Optia Apheresis System. Final target hematocrit was calculated by tracking the number of red cells coming into the system versus the number of red cells removed.
Time frame: upon signing consent to 24 hours post-procedure
Device-related serious adverse events (SAE) in the Full Analysis Set (72 patients).
Terumo BCT
Industry
Evaluation of the Spectra Optia Apheresis Red Blood Cell Exchange Protocol in Patients With Sickle Cell Disease.
Acronym: ESSENTIAL
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