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Completed Not applicable Interventional Results available

Safety and Efficacy of Polymyxin B Hemoperfusion (PMX) for Septic Shock

ClinicalTrials.gov ID: NCT01046669

Public ClinicalTrials.gov record NCT01046669. 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 Jun 26, 2026, 9:31 AM EDT

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

Official title

Evaluating the Use of Polymyxin B Hemoperfusion in a Randomized Controlled Trial of Adults Treated for Endotoxemia and Septic Shock

Study identification

NCT ID
NCT01046669
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Spectral Diagnostics (US) Inc.
Industry
Enrollment
450 participants

Conditions and interventions

Interventions

  • TORAYMYXIN PMX-20R (PMX cartridge) Device
  • Standard medical care for septic shock Other

Device · Other

Eligibility (public fields only)

Age range
18 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
May 31, 2010
Primary completion
Jun 30, 2016
Completion
May 31, 2017
Last update posted
Feb 25, 2019

2010 – 2017

United States locations

U.S. sites
33
U.S. states
27
U.S. cities
33
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Tucson Arizona
Not listed Little Rock Arkansas
Not listed Loma Linda California
Not listed San Diego California
Not listed Stanford California
Not listed Colorado Springs Colorado
Not listed Newark Delaware
Not listed Washington D.C. District of Columbia
Not listed Augusta Georgia
Not listed Idaho Falls Idaho
Not listed Oak Park Illinois
Not listed Peoria Illinois
Not listed Iowa City Iowa
Not listed Hazard Kentucky
Not listed Baltimore Maryland
Not listed Springfield Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Rochester Minnesota
Not listed Jackson Mississippi
Not listed St Louis Missouri
Not listed Omaha Nebraska
Not listed Camden New Jersey
Not listed New York New York
Not listed Greenville North Carolina
Not listed Columbus Ohio
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Chattanooga Tennessee
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Richmond Virginia

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01046669, 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 Feb 25, 2019 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01046669 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →