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

Recruiting Observational Study
Sepsis Septic Shock Immunoparalysis in Septic Shock
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Artcline GmbH · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Subjects ≥ 18 years who are planned to receive ARTICE® treatment during their ICU stay Exclusion Criteria: \-
Contacts

Jens Altrichter, Dr. med.

+49 381 440 703 0

jens.altrichter@artcline.de

CONTACT

Judith Hey, M. Sc.

+49 1772216033

judith.hey@artcline.de

CONTACT