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Completed No phase listed Observational

Patient Plasma Response and Outcome in Septic Shock With Thrombocytopenia Associated Multiple Organ Failure in Children

ClinicalTrials.gov ID: NCT00118664

Public ClinicalTrials.gov record NCT00118664. 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 16, 2026, 5:28 AM 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 purpose of this study is to learn how blood clotting substances respond in children with septic shock, low platelet counts, and multiple organ failure (MOF) treated at different institutions. Multiple organ failure can be related to an infection producing "septic shock," in which substances released in the blood cause poor blood flow to the organs. The number of platelets circulating in your child's blood stream is also decreased (this is called "thrombocytopenia") as a result of this condition. Research has shown that certain substances in the part of the blood known as plasma (the clear liquid part of the blood not including the red blood cells but holding blood clotting factors) can cause the organs to work poorly. The investigators would like to compare these blood responses in children with this condition, receiving a variety of different treatments, for multiple organ failure in other medical centers around the world. The investigators hope to enroll 80 patients into the study.

Study identification

NCT ID
NCT00118664
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
86 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Months to 18 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
Apr 30, 2005
Primary completion
Jan 31, 2012
Completion
Jan 31, 2012
Last update posted
Jun 13, 2016

2005 – 2012

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Children's National Medical Center Washington D.C. District of Columbia 20010
Children's Healthcare of Atlanta at Egleston and Scottish Rite Atlanta Georgia 30322
University of Iowa Children's Hospital Iowa City Iowa 52242
LSU Health Sciences Center Shreveport Louisiana 71130
University of Michigan Medical Center, Mott Children's Hospital Ann Arbor Michigan 48109-0243
Children's Hospitals and Clinics of Minnesota Minneapolis Minnesota 55404
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229
Columbus Childrens Hospital Columbus Ohio 43205
Children's Hospital of Pittsburgh Pittsburgh Pennsylvania 15213
Vanderbilt Children's Hospital Nashville Tennessee 37232
Cook Children's Hospital Fort Worth Texas 76104
Texas Children's Hospital Houston Texas 77030

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 NCT00118664, 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 Jun 13, 2016 · Synced Sep 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00118664 live on ClinicalTrials.gov.

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