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NCT00683007 · ClinicalTrials.gov registry record · NA
Esophageal Echo Assessment of LV Function During Acute Normovolemic Hemodilution Using Crystalloid or Hypertonic Saline
A NA study of Acute Hypovolemia, sponsored by University of California, Davis.
- Completed
- Registry status
- NA
- Development phase
- 9
- Enrollment target
- 1
- Study location
NCT00683007: Completed NA study of Acute Hypovolemia, sponsored by University of California, Davis.
NCT00683007 is a NA study of Acute Hypovolemia that has completed, run by University of California, Davis. The registered enrollment target is 9 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00683007, a NA study of Acute Hypovolemia, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- NA
- Development phase
- 9 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to examine how the heart functions when a calculated amount of blood is removed and how two fluids, Lactated Ringer's (considered the standard replacement fluid) and Hypertonic Saline, re-expand the vascular system.
Conditions Studied
Interventions
- OTHER Volume resuscitation (Crystalloid)
- OTHER Volume resuscitation (Hypertonic Saline Solution)
Study Locations (1)
California
- University of California Davis Medical Center - Sacramento
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9 participants |
| Start Date | 2011-05 |
| Est. Completion | 2012-04 |
| Phase | NA |
What the finished NCT00683007 record still lists
NCT00683007 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 1 condition, with Acute Hypovolemia appearing as the primary indexed condition, and to 2 interventions - of which Volume resuscitation (Crystalloid) is the first listed.
NCT00683007 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT00683007 about?
NCT00683007 is a clinical study titled "Esophageal Echo Assessment of LV Function During Acute Normovolemic Hemodilution Using Crystalloid or Hypertonic Saline". The purpose of this study is to examine how the heart functions when a calculated amount of blood is removed and how two fluids, Lactated Ringer's (considered the standard replacement fluid) and Hypertonic Saline, re-expand the vascular system.
What is the current status of trial NCT00683007?
This trial is currently completed. It is a NA study. The enrollment target is 9 participants. The study started on 2011-05. Estimated completion is 2012-04.
What conditions does trial NCT00683007 study?
This clinical trial studies the following conditions: Acute Hypovolemia.
What interventions are being tested in trial NCT00683007?
The interventions under investigation include: Volume resuscitation (Crystalloid) (OTHER), Volume resuscitation (Hypertonic Saline Solution) (OTHER).
Who is sponsoring clinical trial NCT00683007?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00683007 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00683007's enrollment target sits among peer trials
9 1975th of 2000 higher than 25 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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