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NOT YET RECRUITING
NCT05647096
NA

Safety, Tolerability and Performance of the NucleoCapture Device in the Reduction of Circulating CfDNA/NETs in Subjects with Sepsis

Sponsor: Santersus AG

View on ClinicalTrials.gov

Summary

This is a prospective, multinational, multicentre, randomised, parallel-group, open-label study to assess the safety, tolerability and performance of the NucleoCapture extracorporeal apheresis device in the reduction of circulating cell-free DNA (cfDNA)/Neutrophil Extracellular Traps (NETs) in sepsis patients.

Official title: Safety, Tolerability and Performance of the NucleoCapture Extracorporeal Therapeutic Apheresis Device in the Reduction of Circulating CfDNA/NETs in Subjects with Sepsis

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

73

Start Date

2025-07-01

Completion Date

2027-05-28

Last Updated

2024-11-29

Healthy Volunteers

No

Interventions

DEVICE

NucleoCapture device

100ml NucleoCapture selective DNA adsorber

Locations (9)

University of Bonn

Bonn, Germany

Technical University Dresden

Dresden, Germany

Hannover Medical School

Hannover, Germany

University of Zurich

Zurich, Switzerland

Queen Elizabeth Hospital Birmingham

Birmingham, United Kingdom

Royal Infirmary of Edinburgh

Edinburgh, United Kingdom

Liverpool University Hospital

Liverpool, United Kingdom

Guy's and St Thomas' Hospital

London, United Kingdom

University College London

London, United Kingdom