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NCT00316017 · ClinicalTrials.gov registry record · Phase 3

Hypertonic Resuscitation Following Traumatic Injury

A Phase 3 study, sponsored by University of Washington.

Terminated
Registry status
Phase 3
Development phase
895
Enrollment target

NCT00316017: Clinical Trial Phase 3 study, sponsored by University of Washington.

NCT00316017 is a Phase 3 study that was terminated before completion, run by University of Washington. The registered enrollment target is 895 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (16% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00316017, a Phase 3 study, was terminated before completion, sponsored by University of Washington.

TERMINATED
Registry status
Phase 3
Development phase
895 participants
Enrollment target

Study Summary

The purpose of this study is to determine if hypertonic saline with and without dextran can improve overall survival in victims of trauma with shock. Injury and lost blood from trauma can cause your body to be in shock (low blood pressure related to blood loss). This decreased blood flow can lead to organ damage. In order to restore the blood pressure and blood flow, the medics give fluids into the patients' veins as soon as possible. This is called "resuscitation." The resuscitation fluid most commonly used is "isotonic" or one that is the same concentration as the blood. The investigators are trying to determine if infusing a "hypertonic" fluid (or one more concentrated than the blood) can increase the blood pressure and restore blood flow more efficiently. The hypertonic fluids the investigators are using are called hypertonic saline with dextran (HSD) and hypertonic saline (no dextran). Hypertonic saline is a salt solution that is slightly more concentrated than your blood. Dextran is a sugar solution.

Primary Outcome

The day of episode is counted as "Day 0". So for measures using a 28 day period, the maximum value is 29 (i.e. days 0 through 28).

Interventions

  • DRUG 0.9% normal saline
  • DRUG 7.5% hypertonic saline/6% Dextran-70 (HSD)
  • DRUG 7.5% hypertonic saline (HS)

Trial Details

FieldValue
Enrollment Target 895 participants
Start Date 2006-05
Est. Completion 2009-08
Phase Phase 3
University of Washington

1,048 total trials

Why NCT00316017 stopped before completion

NCT00316017 is an interventional study that assigns participants to a tested intervention. The registered 895 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (16% higher).

The record links to 0 conditions, and to 3 interventions - of which 0.9% normal saline is the first listed.

NCT00316017 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00316017 about?

NCT00316017 is a clinical study titled "Hypertonic Resuscitation Following Traumatic Injury". The purpose of this study is to determine if hypertonic saline with and without dextran can improve overall survival in victims of trauma with shock. Injury and lost blood from trauma can cause your body to be in shock (low blood pressure related to blood loss). This decreased blood flow can lead t...

What is the current status of trial NCT00316017?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 895 participants. The study started on 2006-05. Estimated completion is 2009-08.

What interventions are being tested in trial NCT00316017?

The interventions under investigation include: 0.9% normal saline (DRUG), 7.5% hypertonic saline/6% Dextran-70 (HSD) (DRUG), 7.5% hypertonic saline (HS) (DRUG).

Who is sponsoring clinical trial NCT00316017?

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

How this trial's enrollment target compares

Where NCT00316017's enrollment target sits among peer trials

895 361st of 2000 higher than 1,638 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00316017, the US trial registry maintained by the National Library of Medicine. NCT00316017 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.