Evaluation of the AMICUS RBCx System in Sickle Cell Patients
NCT ID: NCT02372877
Last Updated: 2022-07-29
Study Results
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View full resultsBasic Information
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COMPLETED
NA
83 participants
INTERVENTIONAL
2015-05-31
2018-01-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Amicus Red Cell Exchange in SCD patients
Open arm. Patients with sickle cell disease (SCD) treated using one Amicus Red Cell Exchange procedure.
Amicus Red Cell Exchange in SCD patients
Each patient will be treated with one RBCx procedure using the AMICUS RBCx System
Interventions
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Amicus Red Cell Exchange in SCD patients
Each patient will be treated with one RBCx procedure using the AMICUS RBCx System
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Medically stable subjects who have been previously treated for sickle cell disease with RBC Exchange or RBC Depletion/Exchange.
* Subjects, or subject's legal representative, who have provided signed informed consent, and assent when applicable, prior to participation.
* Adequate availability of sickle trait negative, leukoreduced, Blood type (ABO) blood group, Rhesus factor D (Rh (D)) compatible, unexpired replacement RBC products.
* Subjects with sufficient vascular access to accommodate the RBCx procedure as determined by the medical staff responsible for obtaining intravenous access.
* Subjects who are able and agree to report adverse events (AEs) during the required reporting period.
Exclusion Criteria
* Procedures prescribed within one week of discharge of a hospitalization.
* Subjects with altered mental status that would prohibit the giving and understanding of informed consent, and assent when applicable, who do not have a legally authorized representative.
* Drug abuse, alcohol abuse, or other factors that in the opinion of the investigator could affect the ability of the subject to comply with the requirements of the protocol.
* Subjects who have experienced a serious adverse event associated with an RBCx procedure in the past.
* In the opinion of the investigator, subjects who have a life expectancy fewer than 30 days.
* Subjects who refuse blood products.
* Subjects who are pregnant.
* Subjects who fail to comply with site requirements for cessation of medication that interfere or increase procedure risk.
6 Years
ALL
No
Sponsors
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Versiti
OTHER
Children's Hospital of Philadelphia
OTHER
Barbara Ann Karmanos Cancer Institute
OTHER
University of Texas
OTHER
Washington University School of Medicine
OTHER
Phoenix Children's Hospital
OTHER
Fenwal, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Paul Swerdlow, MD
Role: STUDY_CHAIR
Barbara Ann Karmanos Cancer Institute
Locations
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Phoenix Children's Hospital
Phoenix, Arizona, United States
Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States
Washington University
St Louis, Missouri, United States
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
University of Texas Southwestern Medical Center
Dallas, Texas, United States
BloodCenter of Wisconsin
Milwaukee, Wisconsin, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Other Identifiers
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AMIC-003-CMD
Identifier Type: -
Identifier Source: org_study_id
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