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Terminated Not applicable Interventional Results available

Efficacy Study of a Selective Cytopheretic Device (SCD) in Patients With Acute Kidney Injury

ClinicalTrials.gov ID: NCT01400893

Public ClinicalTrials.gov record NCT01400893. 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 Jul 21, 2026, 4:45 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, Pivotal Study To Assess the Safety and Efficacy of A Selective Cytopheretic Device (SCD) In Patients With Acute Kidney Injury (AKI)

Study identification

NCT ID
NCT01400893
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
SeaStar Medical
Industry
Enrollment
134 participants

Conditions and interventions

Interventions

  • SCD Device

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
Jul 31, 2011
Primary completion
Aug 31, 2013
Completion
Aug 31, 2013
Last update posted
Apr 26, 2021

2011 – 2013

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35233
UCLA Los Angeles California 90025
University of California, San Diego San Diego California 92103
University of Florida Gainesville Florida 32611
University of Florida Jacksonville Florida 32209
Northwestern University Chicago Illinois 60611
University of Iowa Iowa City Iowa 52242
University of Maryland Baltimore Maryland 21201
Massachusetts General Hospital Boston Massachusetts 02114
Beth Isreal Deaconess Medical Center Boston Massachusetts 02215
Baystate Medical Center Springfield Massachusetts 01199
Henry Ford Hospital Detroit Michigan 48202
University of Mississippi Jackson Mississippi 39216
Washington University St Louis Missouri 63110
Albany Medical College Albany New York 12208
Mount Sinai School of Medicine New York New York 10029
Sanford Health Fargo North Dakota 58122
Cleveland Clinic Cleveland Ohio 44195
Medical University Of South Carolina Charleston South Carolina 29425
Memorial Hospital Chattanooga Tennessee 37403
Erlanger Hospital Chattanooga Tennessee 37404
Dallas VA Medical Center Dallas Texas 75216
University of Texas Houston Texas 77030
INOVA Health Care Services Falls Church Virginia 22042
Virginia Commonwealth University Richmond Virginia 23298
University of Wisconsin Madison Wisconsin 53792

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 NCT01400893, 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 Apr 26, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01400893 live on ClinicalTrials.gov.

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