Ignite Creation Date:
2025-12-24 @ 4:13 PM
Ignite Modification Date:
2025-12-25 @ 8:00 PM
Study NCT ID:
NCT01680666
Status:
COMPLETED
Last Update Posted:
2017-11-09
First Post:
2012-08-28
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
A Prospective Trial of Ultrasound Versus Landmark Guided Central Venous Access in the Pediatric Population
Sponsor:
Stanford University
Organization:
Study Overview
Official Title:
A Prospective Randomized Trial of Ultrasound Versus Landmark Guided Central Venous Access in Children
Status:
COMPLETED
Status Verified Date:
2017-10
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:
The investigators hypothesized that, in children undergoing venous cannulation for central line placement by pediatric surgeons, ultrasound-guided cannulation leads to an increase in successful venous cannulation at first attempt compared to landmark guided cannulation.
Detailed Description:
None
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?: