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NCT00750997 · ClinicalTrials.gov registry record

Hypertonic Modulation of Inflammation Following Injury

A clinical trial, sponsored by University of Washington.

Terminated
Registry status
119
Enrollment target

NCT00750997 is a clinical trial that was terminated before completion, run by University of Washington. The registered enrollment target is 119 participants.

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The verdict

NCT00750997 was terminated before completion, sponsored by University of Washington.

TERMINATED
Registry status
119 participants
Enrollment target

Study Summary

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. This study was an ancillary study to the main randomized clinical trial and thus prospective observational in nature 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.

Interventions

  • DRUG hypertonic saline

Trial Details

FieldValue
Enrollment Target 119 participants
Start Date 2007-11
Est. Completion 2009-12

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT00750997

The ClinicalTrials.gov registry entry for NCT00750997 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 119 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which hypertonic saline is the first listed.

NCT00750997 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00750997 about?

NCT00750997 is a clinical study titled "Hypertonic Modulation of Inflammation Following Injury". 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 dysfunction...

What is the current status of trial NCT00750997?

This trial is currently terminated. The enrollment target is 119 participants. The study started on 2007-11. Estimated completion is 2009-12.

What interventions are being tested in trial NCT00750997?

The interventions under investigation include: hypertonic saline (DRUG).

Who is sponsoring clinical trial NCT00750997?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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