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NCT00997321 · ClinicalTrials.gov registry record · Phase 4
Propofol Versus Ketamine for Moderate Procedural Sedation in the Emergency Department (ED)
A Phase 4 study, sponsored by Hennepin Healthcare Research Institute.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
NCT00997321: Completed Phase 4 study, sponsored by Hennepin Healthcare Research Institute.
NCT00997321 is a Phase 4 study that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00997321, a Phase 4 study, has completed, sponsored by Hennepin Healthcare Research Institute.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
Study Summary
This study is a clinical trial of moderate sedation with propofol versus moderate sedation with ketamine for procedural sedation in the Emergency Department.
Primary Outcome
binary measure based on the occurrence of an oxygen saturation less than 93 at any time, a change in baseline end tidal co2 \>10 or an absence on capnographic waveform
Interventions
- DRUG Ketamine
- DRUG propofol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2007-07 |
| Est. Completion | 2009-10 |
| Phase | Phase 4 |
What the finished NCT00997321 record still lists
NCT00997321 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 2 interventions - of which Ketamine is the first listed.
NCT00997321 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00997321 about?
NCT00997321 is a clinical study titled "Propofol Versus Ketamine for Moderate Procedural Sedation in the Emergency Department (ED)". This study is a clinical trial of moderate sedation with propofol versus moderate sedation with ketamine for procedural sedation in the Emergency Department.
What is the current status of trial NCT00997321?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2007-07. Estimated completion is 2009-10.
What interventions are being tested in trial NCT00997321?
The interventions under investigation include: Ketamine (DRUG), propofol (DRUG).
Who is sponsoring clinical trial NCT00997321?
This trial is sponsored by Hennepin Healthcare Research Institute, which has 63 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00997321's enrollment target sits among peer trials
100 770th of 2000 higher than 1,148 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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