A Study Looking At the Use of Biomarkers to Provide Early Indication of Acute Kidney Injury in Patients with Sepsis (Limiting AKI Progression in Sepsis) (LAPIS)

bioMérieux

Status

Terminated

Conditions

Acute Kidney Injury

Septic Shock

Sepsis

Treatments

Device: Subject management guided by NephroCheck® test

Other: Standard of Care

Study type

Interventional

Funder types

Industry

Identifiers

NCT04434209

LAPIS

Details and patient eligibility

About

Biomarkers that provide an early indicator of kidney stress could be useful in clinical practice to detect silent episodes of acute kidney injury (AKI) or for early identification of subjects at risk of AKI. Two urinary biomarkers have been identified as early indicators of AKI. The NephroCheck® test is a commercially available test that uses these biomarkers, and this study assesses the use of these in reducing negative clinical outcomes for patients with sepsis-associated AKI. The study will enroll subjects diagnosed with sepsis, including septic shock, who will be randomly assigned to either receive NephroCheck®-guided kidney-sparing and fast-tracking interventions; or to receive current Standard of Care assessment and treatment.

NOTE: Participants are no longer being recruited to this study.

Enrollment

19 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Clinical diagnosis of sepsis or septic shock.
Admission to the ICU or planned admission to the ICU with an expected stay of 72 hours or more after enrollment in the same hospital.
Expected to have indwelling urinary catheter placed and kept until at least 48 hours after enrollment.
Written informed consent.

Exclusion criteria

Women with known pregnancy, prisoners or institutionalized individuals.
Previous renal transplant.
Stage 2 or 3 Acute Kidney Injury (AKI) at screening.
Receiving dialysis (either acute or chronic), or in imminent need of dialysis at enrollment.
Estimated glomerular filtration rate (eGFR) < 45 mL/min/1.73 m2.
Known End Stage Renal Disease (ESRD) or history of active nephrotic syndrome within the last 3 months.
Known Stage 2-3 AKI within last 2 weeks.
Terminally ill (defined as expectation of death within 6 months), has a do not resuscitate order that would restrict protocol-required procedures, or is being admitted only for palliative care.
History of solid organ transplant and receiving calcineurin inhibitors.
Documented serious allergy (i.e. anaphylaxis) to vancomycin, aminoglycosides, penicillins, or cephalosporins (intravenous or oral).
Known current serum total bilirubin > 4mg/dL.
Subjects already included in an observational study can be co-enrolled in LAPIS. Subjects already included in an interventional study may be enrolled with pre-approval of the sponsor according to the following rules:
1. Co-enrollment in LAPIS will not be allowed with investigational drug and device studies;
2. Studies may be allowed if AKI or kidney function is not an endpoint with pre-approval of the LAPIS sponsor;
3. Co-enrollment in LAPIS will not be allowed if co-enrollment is an exclusion criterion in the other study.
Subjects with laboratory confirmed COVID-19 infection as the primary reason for hospital admission.