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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: Completed Phase 3 study, sponsored by University of Colorado, Denver.
NCT01387139 is a Phase 3 study that has completed, run by University of Colorado, Denver. The registered enrollment target is 183 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
We will record all adverse events during the sedation, and then perform a follow-up call to determine if any additional adverse events occured after discharge.
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 |
What the finished NCT01387139 record still lists
NCT01387139 is an interventional study that assigns participants to a tested intervention. The registered 183 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (76% lower).
The record links to 0 conditions, and to 2 interventions - of which Ketamine is the first listed.
NCT01387139 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01387139's enrollment target sits among peer trials
183 1420th of 2000 higher than 580 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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