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Validation of Progranulin as a Biomarker for Sepsis

Sensitivity and Specificity of Progranulin as a Biomarker for Sepsis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03280576
Acronym
PROGRANULIN
Enrollment
556
Registered
2017-09-12
Start date
2015-04-30
Completion date
2019-06-30
Last updated
2019-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Keywords

Postoperative, Dysfunction Following Cardiac Surgery

Brief summary

Progranulin blood concentrations in patients with sepsis will be analysed in relation to disease status in order to validate progranulin as a biomarker for sepsis. Patients undergoing cardiac surgery will serve as controls.

Detailed description

Single nucleotide polymorphisms with known effects on Progranulin plasma concentrations will be assessed in a separate analysis. Expression levels of microRNAs isolated from plasma, circulating exosomes and blood cells will be determined by next-generation sequencing to characterize epigenetic influences on progranulin plasma levels.

Interventions

None listed

Sponsors

City of Munich
CollaboratorOTHER_GOV
Ludwig-Maximilians - University of Munich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Sepsis or Septic Shock defined according to SEPSIS-3 criteria - Age \> 18 years

Exclusion criteria

* No informed consent * Age \< 18 years * Pregnancy * Immunosuppression (including transplantation) * Charlson Comorbidity Index \> 0 (healthy volunteers)

Design outcomes

Primary

MeasureTime frameDescription
Change in progranulin plasma concentrations during ICU - therapyICU admission, day 1, day 4 of ICU therapyBlood samples will be taken at the abovementioned time points

Secondary

MeasureTime frameDescription
Change in miRNA expression levels in exosomes, serum and blood cells during ICU - therapyICU admission, day 1, day 4 of ICU therapyBlood samples will be taken at the abovementioned time points

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026