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NCT01269307 · ClinicalTrials.gov registry record · NA
Combination Ketamine and Propofol vs Propofol for Emergency Department Sedation: A Prospective Randomized Trial
A NA study, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 99
- Enrollment target
NCT01269307 is a NA study that has completed, run by University of Utah. The registered enrollment target is 99 participants.
The verdict
NCT01269307, a NA study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 99 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if procedural sedation utilizing a 1:1 mixture of propofol and ketamine is equivalent in complications, patient and physician satisfaction, post-procedure pain level, and procedural outcome to propofol sedation alone.
Interventions
- PROCEDURE 1:1 ketamine-propofol mixture sedation
- PROCEDURE Propofol Sedation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 99 participants |
| Start Date | 2010-06 |
| Est. Completion | 2012-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01269307
The ClinicalTrials.gov registry entry for NCT01269307 describes a study currently listed as completed, categorized as NA. 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 Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which 1:1 ketamine-propofol mixture sedation is the first listed.
NCT01269307 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01269307 about?
NCT01269307 is a clinical study titled "Combination Ketamine and Propofol vs Propofol for Emergency Department Sedation: A Prospective Randomized Trial". The purpose of this study is to determine if procedural sedation utilizing a 1:1 mixture of propofol and ketamine is equivalent in complications, patient and physician satisfaction, post-procedure pain level, and procedural outcome to propofol sedation alone.
What is the current status of trial NCT01269307?
This trial is currently completed. It is a NA study. The enrollment target is 99 participants. The study started on 2010-06. Estimated completion is 2012-12.
What interventions are being tested in trial NCT01269307?
The interventions under investigation include: 1:1 ketamine-propofol mixture sedation (PROCEDURE), Propofol Sedation (PROCEDURE).
Who is sponsoring clinical trial NCT01269307?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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