Trials / Completed
CompletedNCT00515359
RCT for Intermittent Versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 276 (actual)
- Sponsor
- Corewell Health West · Academic / Other
- Sex
- All
- Age
- 1 Month – 18 Years
- Healthy volunteers
- Not accepted
Summary
RCT for Intermittent versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies
Detailed description
A study comparing the dose of propofol used as a continuous infusion versus intermittent bolus dosing looking at recovery time complications, and quality of the MRI studies in Pediatric Sedation Services for patients age 1 month to 18 years receiving an brain or spine MRI.
Conditions
- Encephalopathy
- Developmental Delay and Behavioral Changes
- Cord Tumor Compression or Instability
- Cord Tethering or Malformation
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Intermittent Propofol Sedation | Intermittent versus continuous dosage |
| PROCEDURE | Continuous Propofol Sedation | intermittent vs continuous dosage |
Timeline
- Start date
- 2007-06-01
- Primary completion
- 2009-02-01
- Completion
- 2009-02-01
- First posted
- 2007-08-13
- Last updated
- 2024-01-19
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00515359. Inclusion in this directory is not an endorsement.