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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 is a Phase 4 study that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 100 participants.
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.
Interventions
- DRUG Ketamine
- DRUG propofol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2007-07 |
| Est. Completion | 2009-10 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00997321
The ClinicalTrials.gov registry entry for NCT00997321 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hennepin Healthcare Research Institute, which has 63 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ketamine is the first listed.
NCT00997321 reports 0 study locations.
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.
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