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NCT00717574 · ClinicalTrials.gov registry record · NA
Addition of Nitrous Oxide and Its Effects on Depth of Anesthesia
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 32
- Enrollment target
NCT00717574 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 32 participants.
The verdict
NCT00717574, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 32 participants
- Enrollment target
Study Summary
The study hypothesizes that adding 60% nitrous oxide to a steady state sevoflurance or propofol anesthetic will lead to a decrease in both BIS and Entropy indices during a constant level of surgical stimulus
Interventions
- DRUG Sevoflurane group
- DRUG Propofol group
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2008-03 |
| Est. Completion | 2010-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00717574
The ClinicalTrials.gov registry entry for NCT00717574 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Sevoflurane group is the first listed.
NCT00717574 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00717574 about?
NCT00717574 is a clinical study titled "Addition of Nitrous Oxide and Its Effects on Depth of Anesthesia". The study hypothesizes that adding 60% nitrous oxide to a steady state sevoflurance or propofol anesthetic will lead to a decrease in both BIS and Entropy indices during a constant level of surgical stimulus
What is the current status of trial NCT00717574?
This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2008-03. Estimated completion is 2010-10.
What interventions are being tested in trial NCT00717574?
The interventions under investigation include: Sevoflurane group (DRUG), Propofol group (DRUG).
Who is sponsoring clinical trial NCT00717574?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
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