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Terminated Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of the Renal Assist Device in Patients With Acute Renal Failure

ClinicalTrials.gov ID: NCT00280072

Public ClinicalTrials.gov record NCT00280072. 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 Oct 30, 2026, 8:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Controlled, Double-Blind, Phase II Study To Assess Safety and Efficacy With the Renal Assist Device (RAD) in Patients With Acute Renal Failure

Brief summary

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

* The purpose of this study is to evaluate the safety and efficacy of the RAD to determine whether the RAD is effective in reducing mortality in patients with Acute Renal Failure due to Acute Tubule Necrosis and to evaluate the safety of the RAD * If the RAD works normally when used for as long as 72 hours * If the RAD will provide added benefits to normal CVVH therapy for patients with Acute Renal Failure

Study identification

NCT ID
NCT00280072
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
RenaMed Biologics
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Jan 2006 (Type not available)
Primary completion
Aug 2007 (Actual)
Completion
Aug 2007 (Actual)
Last update posted
Dec 3, 2012

2006 – 2007

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35233 —
Denver Nephrologists, PC Denver Colorado 80230 —
George Washington University Hospital Washington D.C. District of Columbia 20037 —
University of Chicago Chicago Illinois 60637 —
Indiana University Indianapolis Indiana 46202 —
University of Maryland Baltimore Maryland 21201 —
Johns Hopkins University Baltimore Maryland 21205 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Brigham & Women's Hospital Boston Massachusetts 02120 —
WNERTA Springfield Massachusetts 01107 —
Mayo Clinic Rochester Minnesota 55905 —
Washington University St Louis Missouri 63110 —
Southeast Renal Associates Charlotte North Carolina 28208 —
Ohio State University Medical Center Columbus Ohio 43210 —
University of Texas Houston Texas 77030 —
Virginia Commonwealth University 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 NCT00280072, 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 Dec 3, 2012 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00280072 live on ClinicalTrials.gov.

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