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NCT02614040 · ClinicalTrials.gov registry record · NA
Saline Against Lactated Ringers or Plasmalyte in the Emergency Department
A NA study of Critical Illness and Acute Kidney Injury, sponsored by Vanderbilt University.
- Completed
- Registry status
- NA
- Development phase
- 14,000
- Enrollment target
- 1
- Study location
NCT02614040 is a NA study of Critical Illness and Acute Kidney Injury that has completed, run by Vanderbilt University. The registered enrollment target is 14,000 participants, above the 2,985-participant average among 91 other Critical Illness trials with a reported enrollment target (369% higher). The trial reports 1 study location across 1 state.
The verdict
NCT02614040, a NA study of Critical Illness and Acute Kidney Injury, has completed, sponsored by Vanderbilt University.
- COMPLETED
- Registry status
- NA
- Development phase
- 14,000 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will be a cluster-randomized, single-center trial comparing 0.9% saline (normal saline) vs physiologically-balanced crystalloid fluids (Lactated Ringers or Plasmalyte A) for intravenous fluid administration in the emergency department.
Conditions Studied
Interventions
- OTHER 0.9% Saline
- OTHER Physiologically-balanced isotonic crystalloid
Study Locations (1)
Tennessee
- Vanderbilt University Medical Center Adult Emergency Department - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14,000 participants |
| Start Date | 2016-01-01 |
| Est. Completion | 2017-06-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02614040
The ClinicalTrials.gov registry entry for NCT02614040 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 14,000 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 2,985-participant average among 91 other Critical Illness trials with a reported enrollment target (369% higher). The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Critical Illness appearing as the primary indexed condition, and to 2 interventions - of which 0.9% Saline is the first listed.
NCT02614040 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT02614040 about?
NCT02614040 is a clinical study titled "Saline Against Lactated Ringers or Plasmalyte in the Emergency Department". This study will be a cluster-randomized, single-center trial comparing 0.9% saline (normal saline) vs physiologically-balanced crystalloid fluids (Lactated Ringers or Plasmalyte A) for intravenous fluid administration in the emergency department.
What is the current status of trial NCT02614040?
This trial is currently completed. It is a NA study. The enrollment target is 14,000 participants. The study started on 2016-01-01. Estimated completion is 2017-06-30.
What conditions does trial NCT02614040 study?
This clinical trial studies the following conditions: Critical Illness, Acute Kidney Injury.
What interventions are being tested in trial NCT02614040?
The interventions under investigation include: 0.9% Saline (OTHER), Physiologically-balanced isotonic crystalloid (OTHER).
Who is sponsoring clinical trial NCT02614040?
This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02614040 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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