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INFLAmmasomes NLRP3 in Platelets and Leukocytes During SEPSIS in Intensive Care Unit (INFLA-SEPSIS)

T

Toulouse University Hospital

Status

Completed

Conditions

Sepsis

Treatments

Other: Blood collection

Study type

Observational

Funder types

Other

Identifiers

NCT04635878
RC31/20/0026
2020-A00593-36 (Other Identifier)

Details and patient eligibility

About

septic shock is the first cause of mortality in intensive care unit. Innate immunity is the body's first line of defense against pathogens

Full description

since their discovery, inflammasomes have an important role during inflammatory response following an aggression. There are intracytoplasmic multiprotein complex activated by cellular stress or infections and is responsible for the release of pro-inflammatory cytokines, including IL-1β. One study focused on the role of the NLRP3 inflammasome in monocyte during sepsis has shown its early alteration that is correlated with mortality. Most studies have analysed inflammasomes in nucleated cells, nevertheless, little is known about inflammasomes in platelets. The aim of the study is to analyze the activation of NLRP3 inflammasome in platelets and leukocytes during sepsis, from patients hospitalized in intensive care unit compare to a control group, until its resolution to better understand the pathophysiology of sepsis

Enrollment

11 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

SEPSIS GROUP:

Inclusion Criteria:

  • hospitalized in intensive care unit with central catheter
  • age > or = 18 years
  • patients suffering from sepsis
  • hospitalized from less than72 hours

Exclusion Criteria:

  • patients with curatorship or guardianship
  • pregnant women
  • patients suffering from malignant blood disease
  • patients suffering from disease associated with NLRP3 inflammasome activation

CONTROL GROUP:

Inclusion Criteria:

  • hospitalized in intensive care unit with central catheter for other reason than infection
  • age > or = 18 years

Exclusion Criteria:

  • patients with infection disease
  • patients with curatorship or guardianship
  • pregnant women
  • patients suffering from malignant blood disease
  • patients suffering from disease associated with NLRP3 inflammasome activation

Trial design

11 participants in 2 patient groups

Sepsis group
Description:
patients suffering from sepsis hospitalized in intensive care unit
Treatment:
Other: Blood collection
Control group
Description:
patients without infection hospitalized in intensive care unit
Treatment:
Other: Blood collection

Trial contacts and locations

1

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Central trial contact

Fanny BOUNES, PH

Data sourced from clinicaltrials.gov

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