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NCT03846596: SEPSIROS

Flow Cytometry Analysis of the Reactive Oxygen Species in Immature Granulocytes in Septic Patient

Terminated Last updated 8 April 2020
What this trial tests

trial testing Additional blood tube in Sepsis in 34 participants. Terminated before completion.

Timeline
26 March 2019
Primary endpoint
10 March 2020
10 March 2020

Quick facts

Lead sponsorUniversity Hospital, Limoges
StatusTerminated
Study typeOBSERVATIONAL
Enrollment34
Start date26 March 2019
Primary completion10 March 2020
Estimated completion10 March 2020
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Limoges

Who can join

18 and older, any sex, with Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Sepsis is life-threatening organ dysfunction caused by a dysregulated host response to infection. Early during sepsis course, immature neutrophils could be found in the bloodstream and may be less efficient than mature neutrophils in reactive oxygen species (ROS) production. ROS induce an oxidative stress for bacteria which can protect through the SOS response. The main objective is to evaluate the level of ROS produced in the early steps of sepsis by the immature neutrophils.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Phagosomal granulocytic ROS in septic patients induce the bacterial SOS response.
    Chollet S, Hernandez Padilla AC, Daix T, Gaschet M, et al · · 2024 · PMID 38799552 · DOI 10.1016/j.isci.2024.109825

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Other recruiting trials for Sepsis

Currently open trials in the same condition.

Other University Hospital, Limoges trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03846596.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing