RecruitingNot ApplicableNCT02235857

Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children

Treatment of Drug-resistant Pediatric Primary Focal Segmental Glomerulosclerosis Using the Liposorber® LA-15 System


Sponsor

Kaneka Medical America LLC

Enrollment

35 participants

Start Date

May 3, 2015

Study Type

INTERVENTIONAL

Conditions

Summary

Liposorber® LA-15 System is a blood purification therapy that selectively removes malignant lipoproteins including low density lipoprotein from circulating blood flow and rapidly reduces the plasma cholesterol level. The system was originally developed for the treatment of patients with serious dyslipidemia such as familial hypercholesterolemia and then applied to improve the dyslipidemia, a common complication of nephrotic syndrome and found to bring about improvement not only with the dyslipidemic condition but the nephrotic condition (e.g, proteinuria and hypoproteinemia). Although the definitive mechanism by which the system may relieve nephrotic syndrome is unknown, it has been recognized as one of alternative therapies for refractory nephrotic syndrome including focal segmental glomerulosclerosis (FSGS) in Japan and referred in the Guidelines for the Treatment of Nephrotic Syndrome endorsed by The Japanese Society of Nephrology. This study is conducted as a post approval study imposed by Humanitarian Device Exemption (HDE) order to confirm the safety and efficacy of the Liposorber® LA-15 System in the treatment of drug-resistant pediatric primary FSGS.


Eligibility

Max Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called LIPOSORBER® LA-15 System for people with focal segmental glomerulosclerosis. The study is currently recruiting participants at 12 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICELIPOSORBER® LA-15 System

LIPOSORBER® LA-15 System is an extracorporeal blood purification system. Approximately 3 to 4 L of plasma is treated in a single treatment session and it takes 2 to 3 hours. Recommended frequency of the treatment is twice weekly for 3 weeks followed by once weekly for 6 weeks, thus it takes 9 weeks for a total of 12 treatment sessions.


Locations(12)

Loma Linda University Children's Hospital

Loma Linda, California, United States

Cedars Sinai Medical Center

Los Angeles, California, United States

Nemours/A.I. duPont Hospital for Children

Wilmington, Delaware, United States

Nemours Children's Health

Orlando, Florida, United States

Helen DeVos Children's Hospital

Grand Rapids, Michigan, United States

University of Minnesota

Minneapolis, Minnesota, United States

Weill Cornell Medical Center / NewYork-Presbyterian

New York, New York, United States

University of North Carolina

Chapel Hill, North Carolina, United States

Akron Children's Hospital

Akron, Ohio, United States

St. Christopher's Hospital for Children

Philadelphia, Pennsylvania, United States

Medical University of South Carolina Children's Hospital

Charleston, South Carolina, United States

Children's Hospital of Richmond at VCU

Richmond, Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT02235857


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