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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 Sep 12, 2026, 9:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. 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
Mar 31, 2012
Primary completion
Nov 30, 2012
Completion
Nov 30, 2012
Last update posted
Oct 14, 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 14, 2014 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01573962 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →