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NCT00734409 · ClinicalTrials.gov registry record · NA
Combining Objective and Subjective Sedation Assessment Tools
A NA study, sponsored by Duke University.
- Completed
- Registry status
- NA
- Development phase
- 300
- Enrollment target
NCT00734409: Completed NA study, sponsored by Duke University.
NCT00734409 is a NA study that has completed, run by Duke University. The registered enrollment target is 300 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00734409, a NA study, has completed, sponsored by Duke University.
- COMPLETED
- Registry status
- NA
- Development phase
- 300 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if the use of a device called the BIS monitor in addition to the Richmond Agitation Sedation Scale will give better assessment of a subject's level of sedation.
Primary Outcome
The mean amount of propofol used on each patient while the patient was in the ICU and receiving mechanical ventilation.
Interventions
- DEVICE Bispectral Index (BIS) Monitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2008-05 |
| Est. Completion | 2011-07 |
| Phase | NA |
What the finished NCT00734409 record still lists
NCT00734409 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower).
The record links to 0 conditions, and to 1 intervention - of which Bispectral Index (BIS) Monitor is the first listed.
NCT00734409 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00734409 about?
NCT00734409 is a clinical study titled "Combining Objective and Subjective Sedation Assessment Tools". The purpose of this study is to determine if the use of a device called the BIS monitor in addition to the Richmond Agitation Sedation Scale will give better assessment of a subject's level of sedation.
What is the current status of trial NCT00734409?
This trial is currently completed. It is a NA study. The enrollment target is 300 participants. The study started on 2008-05. Estimated completion is 2011-07.
What interventions are being tested in trial NCT00734409?
The interventions under investigation include: Bispectral Index (BIS) Monitor (DEVICE).
Who is sponsoring clinical trial NCT00734409?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00734409's enrollment target sits among peer trials
300 330th of 2000 higher than 1,630 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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