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Immune Homeostasis in Sepsis and Septic Shock (IMHOTEP)

C

Charles University, Czech Republic

Status

Enrolling

Conditions

Immunologic Paralysis
Immunologic Suppression
Immune Deficiency
Sepsis

Treatments

Other: transcriptomics
Other: cytokines
Other: flow-cytometry

Study type

Observational

Funder types

Other

Identifiers

NCT04448951
IMHOTEP

Details and patient eligibility

About

Detailed description of immune response and its dynamics in sepsis and septic shock patiens by means of transcriptomics, flow-cytometry and cytokine analysis.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • sepsis/septic shock (SEPSIS-3)
  • age ≥18
  • informed consent
  • inclusion within first 24hrs after development/diagnosis of septic shock

Exclusion criteria

  • disagreement of the patient or legal representative with the entry into the study
  • patients with primary or secondary immunodeficiency
  • presence of active haematological malignancy or an active non-haematological malignancy

Trial design

200 participants in 3 patient groups

sepsis/septic shock
Description:
target population
Treatment:
Other: flow-cytometry
Other: cytokines
Other: transcriptomics
non-septic critically ill
Description:
demographically-matched control group
Treatment:
Other: flow-cytometry
Other: cytokines
Other: transcriptomics
healthy control
Description:
control group
Treatment:
Other: flow-cytometry
Other: cytokines
Other: transcriptomics

Trial contacts and locations

1

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Central trial contact

Thomas Karvunidis, MD, Ph.D.; Marcela Královcová, MD

Data sourced from clinicaltrials.gov

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