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Hypertonic Modulation of Inflammation Following Injury
This study is currently recruiting participants.
Verified by National Institute of General Medical Sciences (NIGMS), September 2008
First Received: September 10, 2008   No Changes Posted
Sponsored by: National Institute of General Medical Sciences (NIGMS)
Information provided by: National Institute of General Medical Sciences (NIGMS)
ClinicalTrials.gov Identifier: NCT00750997
  Purpose

This project seeks to determine the effect of prehospital resuscitation with hypertonic saline vs. conventional crystalloids on the inflammatory response after injury. The leading cause of late mortality following injury is multiple organ dysfunction syndrome (MODS), which results from a dysfunctional inflammatory response after injury. Previous studies suggest that hypertonic saline may be beneficial by modulating this initial response and decreasing subsequent organ injury. This project takes advantage of a unique opportunity, afforded by an NIH-funded multi-center clinical trial of hypertonic resuscitation (conducted by the Resuscitation Outcomes Consortium), to obtain blood samples from patients enrolled in this trial to analyze inflammatory responses early after hypertonic vs. conventional resuscitation.

The proposed study will be carried out in experiments grouped in three Specific Aims: Aim 1 provides a thorough investigation of the immunomodulatory response following hypertonic resuscitation with regard to neutrophil, monocyte, and T cell responses at serial time points after injury and resuscitation. Aim 2 comprises experiments to investigate the mechanisms by which hypertonicity may alter inflammatory cell signaling. Aim 3 seeks to correlate the laboratory findings with clinical endpoints reflective of immune dysfunction including inflammation, organ failure, nosocomial infection, and sepsis.

The investigators hypothesize that hypertonic resuscitation will be associated with modulation of the excessive inflammatory response seen after injury and thus will result in reduced rates of inflammatory organ injury.


Condition
Hemorrhagic Shock
Traumatic Brain Injury

MedlinePlus related topics: Traumatic Brain Injury
U.S. FDA Resources
Study Type: Observational
Study Design: Case Control, Prospective
Official Title: Hypertonic Modulation of Inflammation Following Injury

Further study details as provided by National Institute of General Medical Sciences (NIGMS):

Biospecimen Retention:   Samples Without DNA

Biospecimen Description:

plasma


Estimated Enrollment: 300
Study Start Date: November 2007
Estimated Study Completion Date: March 2010
Groups/Cohorts
I
Hypertonic resuscitation
2
Normal saline resuscitation

  Eligibility

Ages Eligible for Study:   15 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients enrolled in clinical trial of Hypertonic Resuscitation based on prehospital evidence of hypovolemic shock or severe brain injury

Criteria

Inclusion Criteria:

  • Blunt or Penetrating trauma with prehospital systolic blood pressure < 70 or 70-90 mmHg with Heart rate > 108 OR Blunt trauma with prehospital Glasgow coma score <= 8

Exclusion Criteria:

  • Age < 15 yrs
  • Known prisoners
  • Pregnancy
  • Ongoing CPR
  • Burns < 20%
  • Hypothermia < 28 C
  • > 2 liters intravenous fluid prior to study fluid administration
  • > 4 hour from time of dispatch
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00750997

Contacts
Contact: Eileen Bulger, MD 206-744-6448 ebulger@u.washington.edu

Locations
United States, Washington
University of Washington Recruiting
Seattle, Washington, United States, 98104
Principal Investigator: Eileen Bulger, MD            
Canada
University of Toronto Recruiting
Toronto, Canada
Principal Investigator: Sandro Rizoliq, MD            
Sponsors and Collaborators
Investigators
Principal Investigator: Eileen M Bulger, MD University of Washington
  More Information

Additional Information:
No publications provided

Responsible Party: University of Washington ( Eileen M. Bulger, MD )
Study ID Numbers: R01 GM076101-02
Study First Received: September 10, 2008
Last Updated: September 10, 2008
ClinicalTrials.gov Identifier: NCT00750997     History of Changes
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Craniocerebral Trauma
Shock
Wounds and Injuries
Disorders of Environmental Origin
Central Nervous System Diseases
Trauma, Nervous System
Brain Diseases
Hemorrhage
Brain Injuries
Shock, Hemorrhagic
Inflammation

Additional relevant MeSH terms:
Craniocerebral Trauma
Nervous System Diseases
Wounds and Injuries
Central Nervous System Diseases
Disorders of Environmental Origin
Trauma, Nervous System
Hemorrhage
Brain Diseases
Inflammation
Shock, Hemorrhagic
Pathologic Processes
Shock
Brain Injuries

ClinicalTrials.gov processed this record on May 07, 2009