Ignite Creation Date:
2024-05-05 @ 4:38 PM
Last Modification Date:
2024-10-26 @ 9:22 AM
Study NCT ID:
NCT00287560
Status:
COMPLETED
Last Update Posted:
2008-02-25
First Post:
2006-02-06
Brief Title:
Effect of a Modified Propofol Preparation on Injection Pain During Induction of Anesthesia in Children
Sponsor:
B Braun Melsungen AG
Organization:
B Braun Melsungen AG
Study Overview
Official Title:
A Comparison of Venous Tolerability and Injection Pain of a Modified Propofol Preparation and Standard Propofol in the Induction of Anesthesia in Children
Status:
COMPLETED
Status Verified Date:
2008-02
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 purpose of the study is to determine wether a modified propofol preparation shows any effect on the incidence of injection pain in children undergoing elective surgery under general anesthesia
Study hypothesis The use of a modified propofol preparation will reduce the incidence of injection pain in the study group
Study hypothesis The use of a modified propofol preparation will reduce the incidence of injection pain in the study group
Detailed Description:
Pain on injection is the most frequently reported side effect associated with the use of propofol for induction of anesthesia Various measures have been taken to reduce the pain on injection eg administration of lidocaine or fentanyl prior to propofol administration mixture of lidocaine and propofol as well as cooling of the emulsion Although pain on injection had been reduced with some of the above mentioned methods they may not be regarded as a satisfactory solution of the problem
Study Oversight
Has Oversight DMC:
None
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?:
None