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NCT00000254 · ClinicalTrials.gov registry record · Phase 2
Isoflurane at Subanesthetic Concentrations - 6
A Phase 2 study, sponsored by University of Chicago.
- Completed
- Registry status
- Phase 2
- Development phase
- 10
- Enrollment target
NCT00000254 is a Phase 2 study that has completed, run by University of Chicago. The registered enrollment target is 10 participants.
The verdict
NCT00000254, a Phase 2 study, has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 10 participants
- Enrollment target
Study Summary
The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. To test the hypothesis that isoflurane at subanesthetic concentrations does not reduce cold-water immersion pain in healthy volunteers.
Interventions
- OTHER Sham comparator
- DRUG 0.2% isoflurane
- DRUG 0.4% isoflurane
- DRUG 40% Nitrous oxide
- DRUG 0.6% isoflurane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 1995-01 |
| Est. Completion | 1995-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00000254
The ClinicalTrials.gov registry entry for NCT00000254 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Sham comparator is the first listed.
NCT00000254 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00000254 about?
NCT00000254 is a clinical study titled "Isoflurane at Subanesthetic Concentrations - 6". The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. To test the hypothesis that isoflurane at...
What is the current status of trial NCT00000254?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 1995-01. Estimated completion is 1995-09.
What interventions are being tested in trial NCT00000254?
The interventions under investigation include: Sham comparator (OTHER), 0.2% isoflurane (DRUG), 0.4% isoflurane (DRUG), 40% Nitrous oxide (DRUG), 0.6% isoflurane (DRUG).
Who is sponsoring clinical trial NCT00000254?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
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