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NCT04178915

Study of Leukocyte Immunophenotype and the Lipid Transport System as Predictive Biomarkers of Severe Bacterial Infections

ENROLLING BY INVITATION Last updated 11 February 2025
What this trial tests

trial testing Bood leukocyte subsets in Sepsis in 100 participants. Enrolling by invitation.

Timeline
1 July 2019
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorThe Republican Research and Practical Center for Epidemiology and Microbiology
StatusENROLLING BY INVITATION
Study typeOBSERVATIONAL
Enrollment100
Start date1 July 2019
Primary completion31 December 2025
Estimated completion31 December 2025
Sites1 location across Belarus

Drugs / interventions tested

Conditions studied

Sponsor

The Republican Research and Practical Center for Epidemiology and Microbiology — full company profile →

Who can join

Adults 18 to 60, any sex, with Sepsis or Infective Endocarditis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Current study evaluates the relationship between cell immunity and lipid transport systems in patients with severe bacterial infections (on the model of pneumonia, infective endocarditis, sepsis) in order to develop new methods for predicting the course and outcome of severe bacterial infections.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Bood leukocyte subsets

Trials testing the same drug.

Other recruiting trials for Sepsis

Currently open trials in the same condition.

Other The Republican Research and Practical Center for Epidemiology and Microbiology 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/NCT04178915.

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