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NCT00997126 · ClinicalTrials.gov registry record · Phase 4
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation
A Phase 4 study of Sedation, sponsored by Hennepin Healthcare Research Institute.
- Completed
- Registry status
- Phase 4
- Development phase
- 126
- Enrollment target
- 1
- Study location
NCT00997126: Completed Phase 4 study of Sedation, sponsored by Hennepin Healthcare Research Institute.
NCT00997126 is a Phase 4 study of Sedation that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 126 participants, below the 100,175-participant average among 12 other Sedation trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00997126, a Phase 4 study of Sedation, has completed, sponsored by Hennepin Healthcare Research Institute.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 126 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a clinical trial of propofol and alfentanil as agents for moderated procedural sedation in patients undergoing sedation in the emergency department (ED).
Conditions Studied
Interventions
- DRUG Propofol
- DRUG Alfentanil
Study Locations (1)
Minnesota
- Hennepin County Medical Center - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 126 participants |
| Start Date | 2009-10 |
| Est. Completion | 2015-04 |
| Phase | Phase 4 |
What the finished NCT00997126 record still lists
NCT00997126 is an interventional study that assigns participants to a tested intervention. The registered 126 participants enrollment target is mid-sized for trials with a published cap, below the 100,175-participant average among 12 other Sedation trials with a reported enrollment target (100% lower).
The record links to 1 condition, with Sedation appearing as the primary indexed condition, and to 2 interventions - of which Propofol is the first listed.
NCT00997126 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT00997126 about?
NCT00997126 is a clinical study titled "Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation". This is a clinical trial of propofol and alfentanil as agents for moderated procedural sedation in patients undergoing sedation in the emergency department (ED).
What is the current status of trial NCT00997126?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 126 participants. The study started on 2009-10. Estimated completion is 2015-04.
What conditions does trial NCT00997126 study?
This clinical trial studies the following conditions: Sedation.
What interventions are being tested in trial NCT00997126?
The interventions under investigation include: Propofol (DRUG), Alfentanil (DRUG).
Who is sponsoring clinical trial NCT00997126?
This trial is sponsored by Hennepin Healthcare Research Institute, which has 63 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00997126 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Sedation
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00997126's enrollment target sits among peer trials
126 7th of 12 higher than 6 of 12 other Sedation trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Sedation 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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A Pooled Analysis of Long-Term Outcomes After Inhaled Isoflurane Via the Sedaconda ACD-S Compared to Intravenous Propofol
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