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

A

Artcline

Status

Enrolling

Conditions

Immunoparalysis in Septic Shock
Septic Shock
Sepsis

Study type

Observational

Funder types

Industry

Identifiers

NCT07388628
ARTistry

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects ≥ 18 years who are planned to receive ARTICE® treatment during their ICU stay

Exclusion criteria

-

Trial contacts and locations

1

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Central trial contact

Judith Gross, M. Sc.; Jens Altrichter, Dr. med.

Data sourced from clinicaltrials.gov

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