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Determination of the Nature of the Endogenous Ligand of TREM-1 and Its Use as a New Diagnostic Biomarker in Sepsis

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Withdrawn

Conditions

Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT01903668
Ducoroy PHRC IR 2012

Details and patient eligibility

About

Step 1: Identification and characterisation of the TREM1L protein from samples already available characterised at the hospital Central of Nancy Step 2: Study of the isoforms of TREM1L in correlation with the prognosis of sepsis, Step 3: implementation of assay methods for TREM1L (ELISA or SUPRA MS) Step 4: Validation of assays for TREM1L and its isoforms in a larger number of subjects (inclusion of samples from Dijon CHU and Besançon CHU)

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients hospitalised in a Medical Intensive Care unit whatever the reason
  • written informed consent obtained

Exclusion criteria

  • patients less than 18 years old or under guardianship, persons without national health insurance.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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