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NCT00151307 · ClinicalTrials.gov registry record · Phase 2
Effects of Cerebral Oxygen Saturation on Neuropsychological Outcomes
A Phase 2 study, sponsored by Weill Medical College of Cornell University.
- Terminated
- Registry status
- Phase 2
- Development phase
- 200
- Enrollment target
NCT00151307: Clinical Trial Phase 2 study, sponsored by Weill Medical College of Cornell University.
NCT00151307 is a Phase 2 study that was terminated before completion, run by Weill Medical College of Cornell University. The registered enrollment target is 200 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00151307, a Phase 2 study, was terminated before completion, sponsored by Weill Medical College of Cornell University.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the effects of maintaining adequate cerebral oxygen saturation (over 40%) on patients undergoing cardiac surgery. Effects on neuropsychological outcome, length of ICU stay, and length of hospital stay will be measured.
Interventions
- DEVICE INVOS cerebral oximeter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2001-02 |
| Est. Completion | 2007-04 |
| Phase | Phase 2 |
Why NCT00151307 stopped before completion
NCT00151307 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% higher).
The record links to 0 conditions, and to 1 intervention - of which INVOS cerebral oximeter is the first listed.
NCT00151307 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00151307 about?
NCT00151307 is a clinical study titled "Effects of Cerebral Oxygen Saturation on Neuropsychological Outcomes". The purpose of this study is to evaluate the effects of maintaining adequate cerebral oxygen saturation (over 40%) on patients undergoing cardiac surgery. Effects on neuropsychological outcome, length of ICU stay, and length of hospital stay will be measured.
What is the current status of trial NCT00151307?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2001-02. Estimated completion is 2007-04.
What interventions are being tested in trial NCT00151307?
The interventions under investigation include: INVOS cerebral oximeter (DEVICE).
Who is sponsoring clinical trial NCT00151307?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00151307's enrollment target sits among peer trials
200 304th of 2000 higher than 1,652 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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