Viewing Study NCT00515359


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Study NCT ID: NCT00515359
Status: COMPLETED
Last Update Posted: 2024-01-19
First Post: 2007-08-07
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: RCT for Intermittent Versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies
Sponsor: Corewell Health West
Organization:

Study Overview

Official Title: RCT for Intermittent Versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies
Status: COMPLETED
Status Verified Date: 2024-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: