Premarket Clinical Safety Assessment of the ELISIO™-HX

NARecruitingINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

September 8, 2025

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Renal FailureAcute Renal FailureChronic Renal FailureChronic Kidney DiseasesEnd Stage Renal Disease
Interventions
DEVICE

ELISIO™-HX Dialyzer

Following consent, participants will undergo a baseline hemodialysis treatment with their currently used dialyzer, the ELISIO-H™, and following the baseline visit will receive hemodialysis with the investigational device, ELISIO™-HX, three times a week for 12 weeks.

Trial Locations (1)

23517

RECRUITING

Davita Clinical Research, Norfolk

Sponsors
All Listed Sponsors
collaborator

Bright Research Partners

INDUSTRY

lead

Nipro Medical Corporation

INDUSTRY

NCT07058909 - Premarket Clinical Safety Assessment of the ELISIO™-HX | Biotech Hunter | Biotech Hunter