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NCT00535613 · ClinicalTrials.gov registry record · Phase 4
Propofol in Emergence Agitation
A Phase 4 study, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- Phase 4
- Development phase
- 99
- Enrollment target
NCT00535613 is a Phase 4 study that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 99 participants.
The verdict
NCT00535613, a Phase 4 study, has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 99 participants
- Enrollment target
Study Summary
The purpose of the study is to see if a small dose of propofol given intravenously (through a needle into a vein) at the end of anesthesia can make it less likely that children will be agitated as the come out of the anesthetic.
Interventions
- DRUG Propofol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 99 participants |
| Start Date | 2007-08 |
| Est. Completion | 2010-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00535613
The ClinicalTrials.gov registry entry for NCT00535613 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Propofol is the first listed.
NCT00535613 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00535613 about?
NCT00535613 is a clinical study titled "Propofol in Emergence Agitation". The purpose of the study is to see if a small dose of propofol given intravenously (through a needle into a vein) at the end of anesthesia can make it less likely that children will be agitated as the come out of the anesthetic.
What is the current status of trial NCT00535613?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 99 participants. The study started on 2007-08. Estimated completion is 2010-12.
What interventions are being tested in trial NCT00535613?
The interventions under investigation include: Propofol (DRUG).
Who is sponsoring clinical trial NCT00535613?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
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