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Dynamics of Organ Damage and Immune Exhaustion During Sepsis

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Mayo Clinic

Status

Enrolling

Conditions

Sepsis

Treatments

Other: Observation

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06817408
24-009707
7R35GM142710-04 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This is a prospective, non-randomized study investigating if organ damage and immune changes can be measured by liquid biopsy NGS through advanced analytical methods.

Full description

To determine the sample size needed to derive a signature matrix to identify novel biomarkers in sepsis, investigators performed a mathematical modeling exercise of the lower limits of sensitivity of this liquid biopsy approach. The detection limit of cell-free nucleic acid analysis is determined in part by the number of independent transcripts or "reporters" that are interrogated. Using an established and independently validated binomial model that was previously applied to the prediction of circulating tumor nucleic acid detection limits, investigators estimated the probability of cell-free nucleic acid detection in sepsis patients based on the number of unique tissue-specific reporters (i.e., hepatic transcripts that may reflect disease severity). This yields a result of n=18 per group to achieve 0.90 power at alpha=0.05. The investigators will thus plan to analyze data from n=18 per cell/tissue type to derive the signature matrix for this project.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Patients who've developed a shocked state (Hypotension or Lactate grade >4) or Clinical Concern

Exclusion criteria

  • <18 years of age
  • Pregnant Women
  • Nursing women

Trial contacts and locations

1

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Central trial contact

Derek E Vanmeter

Data sourced from clinicaltrials.gov

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