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NCT00848991 · ClinicalTrials.gov registry record · Phase 3
Comparison of Propofol to Precedex With Propofol for Emergence and Recovery in Patients Having Craniotomy Surgery
A Phase 3 study, sponsored by The Cooper Health System.
- Completed
- Registry status
- Phase 3
- Development phase
- 15
- Enrollment target
NCT00848991: Completed Phase 3 study, sponsored by The Cooper Health System.
NCT00848991 is a Phase 3 study that has completed, run by The Cooper Health System. The registered enrollment target is 15 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00848991, a Phase 3 study, has completed, sponsored by The Cooper Health System.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 15 participants
- Enrollment target
Study Summary
Primary Hypothesis: The use of a Precedex infusion, in addition to propofol during surgery, will improve patient management through the anesthesia postoperative recovery period determined by improvement in patients? tolerance of the endotracheal tube. Secondary hypothesis: The use of a Precedex infusion, in addition to propofol during surgery will provide improved hemodynamic stability.
Interventions
- DRUG Propofol
- DRUG Precedex
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2009-02 |
| Est. Completion | 2010-02 |
| Phase | Phase 3 |
What the finished NCT00848991 record still lists
NCT00848991 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 2 interventions - of which Propofol is the first listed.
NCT00848991 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00848991 about?
NCT00848991 is a clinical study titled "Comparison of Propofol to Precedex With Propofol for Emergence and Recovery in Patients Having Craniotomy Surgery". Primary Hypothesis: The use of a Precedex infusion, in addition to propofol during surgery, will improve patient management through the anesthesia postoperative recovery period determined by improvement in patients? tolerance of the endotracheal tube. Secondary hypothesis: The use of a Precedex inf...
What is the current status of trial NCT00848991?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 15 participants. The study started on 2009-02. Estimated completion is 2010-02.
What interventions are being tested in trial NCT00848991?
The interventions under investigation include: Propofol (DRUG), Precedex (DRUG).
Who is sponsoring clinical trial NCT00848991?
This trial is sponsored by The Cooper Health System, which has 39 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00848991's enrollment target sits among peer trials
15 1977th of 2000 higher than 18 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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