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NCT01387139 · ClinicalTrials.gov registry record · Phase 3
Ketamine Versus Co-administration of Ketamine and Propofol for Procedural Sedation in a Pediatric Emergency Department
A Phase 3 study, sponsored by University of Colorado, Denver.
- Completed
- Registry status
- Phase 3
- Development phase
- 183
- Enrollment target
NCT01387139 is a Phase 3 study that has completed, run by University of Colorado, Denver. The registered enrollment target is 183 participants.
The verdict
NCT01387139, a Phase 3 study, has completed, sponsored by University of Colorado, Denver.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 183 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the effectiveness of the co-administration of intravenous ketamine and propofol to intravenous ketamine as a single agent for procedural sedation in the pediatric emergency department. The investigators hypothesize that patients receiving co-administration of ketamine and propofol will have a lower rate of adverse events, compared to patients receiving ketamine for procedural sedation.
Interventions
- DRUG Ketamine
- DRUG Ketamine Co-administered with Propofol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 183 participants |
| Start Date | 2011-01 |
| Est. Completion | 2017-11-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01387139
The ClinicalTrials.gov registry entry for NCT01387139 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 183 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ketamine is the first listed.
NCT01387139 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01387139 about?
NCT01387139 is a clinical study titled "Ketamine Versus Co-administration of Ketamine and Propofol for Procedural Sedation in a Pediatric Emergency Department". The purpose of this study is to compare the effectiveness of the co-administration of intravenous ketamine and propofol to intravenous ketamine as a single agent for procedural sedation in the pediatric emergency department. The investigators hypothesize that patients receiving co-administration of ...
What is the current status of trial NCT01387139?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 183 participants. The study started on 2011-01. Estimated completion is 2017-11-03.
What interventions are being tested in trial NCT01387139?
The interventions under investigation include: Ketamine (DRUG), Ketamine Co-administered with Propofol (DRUG).
Who is sponsoring clinical trial NCT01387139?
This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.
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