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Early Diagnostic of Sepsis and Potential Impact on Antibiotic Management Based on Serial.Pancreatic Stone Protein (PSP) Measured Using the AbioScope.

A

Abionic

Status

Completed

Conditions

Sepsis

Treatments

Device: Blood sampling

Study type

Observational

Funder types

Industry

Identifiers

NCT03474809
AB-PSP-001

Details and patient eligibility

About

The main purpose of this study is to compare the early detection of sepsis and the decision, by the Investigator to start or not, or to change, antibiotics in Intensive Care Unit (ICU) patients at high risk of sepsis, based on standard of care (clinical, laboratory and imaging data but not on PSP values), as well as timing of antibiotic de-escalation versus the the retrospective assessment (i.e., at the end of the study) of a First Endpoint Adjudication Committee (EAC) which is aware of the clinical data and of the PSP values but not of the Investigator's decision(s), and of the retrospective assessment of a Second Endpoint Adjudication Committee which is only aware of the PSP values.

This study will follow the site's routine clinical practice for the diagnostic, assessment and treatment of the enrolled patients, with the exception of daily blood samples which will be taken for the PSP measurement using the AbioScope as well as another daily sample taken for central analysis of biomarkers of inflammation, infection and/or sepsis (including but not limited to C-reactive protein [CRP] and Procalcitonin [PCT]).

Enrollment

296 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult patients (age ≥ 18 years)
  2. Requiring ICU management
  3. At high risk of sepsis (septic patients are excluded)
  4. Expected ICU stay for more than 4 days
  5. Have provided written informed consent or consent is given by the patient's legally designated representative.

Exclusion criteria

  1. Patient expected to die within 48 hours of admission to ICU
  2. Patient suffering from or known acute or chronic pancreatitis, pancreatic cancer or admitted after pancreatectomy, but if a patient develops any pancreatic disease during the IUC stay he/she will remain in the study.

Trial contacts and locations

14

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Data sourced from clinicaltrials.gov

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