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Completed No phase listed Observational

A Sample Collection Study to Validate the Astute Medical NephroCheck Test in Critically Ill Subjects at Risk for Acute Kidney Injury

ClinicalTrials.gov ID: NCT01573962

Public ClinicalTrials.gov record NCT01573962. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 5, 2026, 6:01 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this sample collection study is to collect blood and urine samples. This study is observational and will have no impact on the medical management of the subject.

Study identification

NCT ID
NCT01573962
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Astute Medical, Inc.
Industry
Enrollment
420 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2012 (Type not available)
Primary completion
Dec 2012 (Actual)
Completion
Dec 2012 (Actual)
Last update posted
Oct 15, 2014

2012

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
21
Facility City State ZIP Site status
Not listed Loma Linda California 92354 —
Not listed Los Angels California 90095 —
Not listed Washington D.C. District of Columbia 20037 —
Not listed Gainesville Florida 32610-0254 —
Not listed Tampa Florida 33606 —
Not listed Idaho Falls Idaho 83404 —
Not listed Chicago Illinois 60611 —
Not listed Chicago Illinois 60637 —
Not listed Shreveport Louisiana 71103 —
Not listed Baltimore Maryland 21201 —
Not listed Ann Arbor Michigan 48109 —
Not listed Minneapolis Minnesota 55415 —
Not listed Missoula Montana 59802 —
Not listed Rochester New York 14621 —
Not listed The Bronx New York 10467 —
Not listed Durham North Carolina 27705 —
Not listed Akron Ohio 44309 —
Not listed Portland Oregon 97239 —
Not listed Pittsburgh Pennsylvania 15212 —
Not listed Pittsburgh Pennsylvania 15261 —
Not listed Nashville Tennessee 37232 —
Not listed Houston Texas 77030 —
Not listed Richmond Virginia 23298 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01573962, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2014 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01573962 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →