ARTICE® Real Data Collection & Observational Trial, Phase 4 Study

NCT07388628 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-02-09

No results posted yet for this study

Summary

The objectives of this registry study are to:

1. Record real-life data related to the use of the ARTICE® therapy in sepsis subjects.
2. Further evaluate ARTICE® treatment efficacy.
3. Identify potential sub-groups, assess their risk-benefit- and safety profile.
4. Changes in SOFA score D0 to SOFA Score D7.

Conditions

  • Sepsis
  • Septic Shock
  • Immunoparalysis in Septic Shock

Sponsors & Collaborators

  • Artcline GmbH

    lead INDUSTRY

Principal Investigators

  • Martin Sauer, Prof. Dr. med. · Klinikum Magdeburg, Klinik für Intensiv- & Rettungsmedizin

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-25
Primary Completion
2027-09-30
Completion
2027-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07388628 on ClinicalTrials.gov