Multicenter Symphony IL-6 Monitoring Sepsis ICU Study

NCT06181604 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 143

Last updated 2025-08-03

No results posted yet for this study

Summary

The primary objective of this study is to establish an IL-6 concentration cutoff and optimal time point(s) for using Symphony IL-6 that predict 28-day mortality in patients who are admitted or are intended to be admitted to the intensive care unit (ICU) diagnosed with sepsis or septic shock.

Conditions

Sponsors & Collaborators

  • Bluejay Diagnostics, Inc.

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-12
Primary Completion
2024-07-12
Completion
2024-07-12

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06181604 on ClinicalTrials.gov