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NCT00708526 · ClinicalTrials.gov registry record · NA
Improved Patient Recovery After Anesthesia With Hypercapnia Hyperpnoea
A NA study, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 22
- Enrollment target
NCT00708526 is a NA study that has completed, run by University of Utah. The registered enrollment target is 22 participants.
The verdict
NCT00708526, a NA study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 22 participants
- Enrollment target
Study Summary
The proposed study will measure the time from the end of surgery until the time patients meet the discharge criteria from the postoperative anesthesia care unit and the time from the end of surgery until the patients regained cognitive function after anesthesia.
Interventions
- OTHER standard of care for phase one anesthesia care
- DEVICE Quick Emergence Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2008-03 |
| Est. Completion | 2008-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00708526
The ClinicalTrials.gov registry entry for NCT00708526 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which standard of care for phase one anesthesia care is the first listed.
NCT00708526 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00708526 about?
NCT00708526 is a clinical study titled "Improved Patient Recovery After Anesthesia With Hypercapnia Hyperpnoea". The proposed study will measure the time from the end of surgery until the time patients meet the discharge criteria from the postoperative anesthesia care unit and the time from the end of surgery until the patients regained cognitive function after anesthesia.
What is the current status of trial NCT00708526?
This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2008-03. Estimated completion is 2008-11.
What interventions are being tested in trial NCT00708526?
The interventions under investigation include: standard of care for phase one anesthesia care (OTHER), Quick Emergence Device (DEVICE).
Who is sponsoring clinical trial NCT00708526?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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