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Completed

NCT Number: NCT01736657

Evaluation of Spectra Optia Red Blood Cell Exchange in Sickle Cell Patients

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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Key information

Age range

12 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's of Alabama, Birmingham, Alabama, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 12 years old
  • Enrolled in a program of regular red blood cell exchange (RBCx) to prevent symptoms/complications of sickle cell disease (SCD) or Initiating a program of regular RBCx or Receiving RBCx as a pre-surgical procedure.
  • Medically stable
  • Previous documentation of diagnosis by hemoglobin electrophoresis of a type of sickle cell disorder requiring RBCx.
  • Sufficient vascular access to accommodate the RBCx procedure as determined by the apheresis technician performing the procedure or phlebotomist responsible for obtaining intravenous access.
  • Availability of sickle trait negative, leukoreduced, ABO blood group, Rhesus factor D (Rh (D)) compatible, unexpired replacement blood. See Glossary for definition of replacement blood.
  • Able to commit to the study follow-up schedule.
  • Agree to report adverse events (AEs) during the required reporting period.

Exclusion criteria

  • Inability to obtain informed consent/assent from patient, or permission from parent or guardian.
  • Pregnancy (negative serum pregnancy test required for females of childbearing potential).
  • Life expectancy is fewer than 30 days from time of procedure.
  • Incarcerated or a ward of the court.
  • Refusal of blood products.
  • Failure to comply with site standard requirements for cessation of medications (e.g., angiotensin converting enzyme (ACE) inhibitors) that interfere with or increase risk of RBCx procedures.
  • History of drug or alcohol abuse that, in the opinion of the investigator, could affect the ability of the patient to comply with the study requirements Inability to comply with the protocol in the opinion of the investigator.

Treatment and study plan

Red blood cell exchange in sickle cell

Device

One Red Blood Cell Exchange using Spectra Optia Apheresis System per enrolled patient

Other names: Specta Optia Apheresis System

Primary outcomes

  1. Mean Ratio 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)

    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.

Secondary outcomes

  1. Procedural Success of the Spectra Optia System in the Evaluable Population

    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).

  2. Spectra Optia System's Ability to Achieve the Desired Final Hematocrit in the Evaluable Population

    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.

  3. Device-related Serious Adverse Events (SAE) in the Full Analysis Set

    Time frame: upon signing consent to 24 hours post-procedure

    Device-related serious adverse events (SAE) in the Full Analysis Set (72 patients).

Sponsors and collaborators

Lead sponsor

Terumo BCT

Industry

Registry information

Official study title

Evaluation of the Spectra Optia Apheresis Red Blood Cell Exchange Protocol in Patients With Sickle Cell Disease.

Acronym: ESSENTIAL

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Nov 29, 2012
Registry last updated
Jul 14, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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