Initial Feasibility Study of the CycloPE® Device

NAActive, not recruitingINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

June 11, 2024

Primary Completion Date

April 26, 2025

Study Completion Date

May 15, 2025

Conditions
SepsisInfectionBacteremia SepsisSystemic Inflammatory Response Syndrome (SIRS)
Interventions
DEVICE

PATH EX CycloPE® Device

Participants in this arm will receive two extracorporeal blood filtration treatments using the PATH EX CycloPE® device. The first treatment will be initiated following baseline assessments, and the second treatment will occur 24-36 hours after the start of the first treatment. Each treatment will last up to 4 hours. The device is designed to target and remove bacteria from the bloodstream. All participants will also receive standard-of-care treatment for sepsis, including IV antibiotics, as determined by the treating physician.

Trial Locations (1)

0087

Erebuni Medical Cener, Yerevan

All Listed Sponsors
lead

PATH EX, Inc.

INDUSTRY

NCT06970899 - Initial Feasibility Study of the CycloPE® Device | Biotech Hunter | Biotech Hunter