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NCT02404610 · ClinicalTrials.gov registry record · Phase 4
Moderate Versus Deep Procedural Sedation With Propofol in the Emergency Department
A Phase 4 study of Pain, sponsored by Hennepin Healthcare Research Institute.
- Completed
- Registry status
- Phase 4
- Development phase
- 107
- Enrollment target
- 1
- Study location
NCT02404610: Completed Phase 4 study of Pain, sponsored by Hennepin Healthcare Research Institute.
NCT02404610 is a Phase 4 study of Pain that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 107 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (65% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02404610, a Phase 4 study of Pain, has completed, sponsored by Hennepin Healthcare Research Institute.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 107 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is a clinical trial of moderate sedation versus deep sedation with propofol for procedural sedation in the Emergency Department. The purpose of this study is to compare the rate of amnesia and respiratory depression rate in patients who receive moderate sedation to those that receive deep sedation.
Primary Outcome
adverse respiratory events measured using capnography, pulse oximetry, and airway maneuvers performed during the sedation procedure
Conditions Studied
Interventions
- PROCEDURE Moderate Procedural Sedation with a sedative medication.
- PROCEDURE Deep Procedural Sedation with a sedative medication.
- DRUG propofol
Study Locations (1)
Minnesota
- Hennepin County Medical Center - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 107 participants |
| Start Date | 2014-07 |
| Est. Completion | 2018-12-01 |
| Phase | Phase 4 |
What the finished NCT02404610 record still lists
NCT02404610 is an interventional study that assigns participants to a tested intervention. The registered 107 participants enrollment target is mid-sized for trials with a published cap, below the 304-participant average among 374 other Pain trials with a reported enrollment target (65% lower).
The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 3 interventions - of which Moderate Procedural Sedation with a sedative medication. is the first listed.
NCT02404610 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT02404610 about?
NCT02404610 is a clinical study titled "Moderate Versus Deep Procedural Sedation With Propofol in the Emergency Department". This study is a clinical trial of moderate sedation versus deep sedation with propofol for procedural sedation in the Emergency Department. The purpose of this study is to compare the rate of amnesia and respiratory depression rate in patients who receive moderate sedation to those that receive deep...
What is the current status of trial NCT02404610?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 107 participants. The study started on 2014-07. Estimated completion is 2018-12-01.
What conditions does trial NCT02404610 study?
This clinical trial studies the following conditions: Pain.
What interventions are being tested in trial NCT02404610?
The interventions under investigation include: Moderate Procedural Sedation with a sedative medication. (PROCEDURE), Deep Procedural Sedation with a sedative medication. (PROCEDURE), propofol (DRUG).
Who is sponsoring clinical trial NCT02404610?
This trial is sponsored by Hennepin Healthcare Research Institute, which has 63 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02404610 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 Pain
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 NCT02404610's enrollment target sits among peer trials
107 156th of 374 higher than 219 of 374 other Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain 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.
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