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NOT YET RECRUITING
NCT06258291
NA

First in Human Trial to Assess the Feasibility and Preliminary Safety of Adjunctive Treatment with the HemoSystem REBOOT in Critically Ill Patients with Sepsis-induced Immunosuppression

Sponsor: hemotune AG

View on ClinicalTrials.gov

Summary

The aim of this randomized controlled trial is to restore immune function by selectively removing three mediators largely contributing to sepsis-induced immunosuppression from extracorporeal circulation.

Official title: A Multi-center Randomized Controlled First in Human Trial to Assess the Feasibility and Preliminary Safety Data of Adjunctive Treatment with the HemoSystem REBOOT in Critically Ill PatientS with Sepsis-induced ImmunOsuppREssion (RESTORE I)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

16

Start Date

2025-09-01

Completion Date

2026-12-30

Last Updated

2025-03-14

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Hemosystem REBOOT

The HemoSystem REBOOT will selectively remove three mediators largely contributing to sepsis-induced immunosuppression, from extracorporeal circulation based on magnetic beads.

Locations (2)

University Hospital Bern Inselspital

Bern, Switzerland

University Hospital Zurich

Zurich, Switzerland