Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING

Establishment of ProNephro AKI (NGAL) Cut Off Value for Risk Assessment of Moderate to Severe Acute Kidney Injury in Adults

NCT06652100 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research is to collect blood and urine from adult patients admitted to an intensive care unit. This is to assess the performance of the ProNephro AKI (NGAL) assay (lab test) as an aid to identify patients at risk for acute kidney injury.

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST ProNephro AKI (NGAL)

Study Locations (12)

Alabama

  • The University of Alabama — Birmingham

California

  • UC Davis — Sacramento

Connecticut

  • Yale University — New Haven

Illinois

  • University of Chicago — Chicago

Maryland

  • Johns Hopkins University — Baltimore

Massachusetts

  • Massachusetts General Hospital — Boston

Michigan

  • University of Michigan — Ann Arbor

New Mexico

  • University of New Mexico — Albuquerque

Trial Details

FieldValue
Enrollment Target 800 participants
Start Date 2024-10-28
Est. Completion 2026-01-31

Sponsor

BioPorto Diagnostics

2 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06652100

The ClinicalTrials.gov registry entry for NCT06652100 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BioPorto Diagnostics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acute Kidney Injury appearing as the primary indexed condition, and to 1 intervention — of which ProNephro AKI (NGAL) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06652100 reports 12 study locations spanning 12 distinct geographic areas — top geographies include Alabama, California, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06652100 about?

NCT06652100 is a clinical study titled "Establishment of ProNephro AKI (NGAL) Cut Off Value for Risk Assessment of Moderate to Severe Acute Kidney Injury in Adults". The purpose of this research is to collect blood and urine from adult patients admitted to an intensive care unit. This is to assess the performance of the ProNephro AKI (NGAL) assay (lab test) as an aid to identify patients at risk for acute kidney injury.

What is the current status of trial NCT06652100?

This trial is currently active not recruiting. The enrollment target is 800 participants. The study started on 2024-10-28. Estimated completion is 2026-01-31.

What conditions does trial NCT06652100 study?

This clinical trial studies the following conditions: Acute Kidney Injury. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06652100?

The interventions under investigation include: ProNephro AKI (NGAL) (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06652100?

This trial is sponsored by BioPorto Diagnostics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06652100 being conducted?

This trial has 12 study locations across Alabama, California, Connecticut, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial