Viewing Study NCT00126919



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Study NCT ID: NCT00126919
Status: COMPLETED
Last Update Posted: 2012-02-09
First Post: 2005-08-03

Brief Title: Reduction of Topical Anesthetic Time for Subcutaneous Port Access Using Ultrasound
Sponsor: Connecticut Childrens Medical Center
Organization: Connecticut Childrens Medical Center

Study Overview

Official Title: Randomized Crossover Trial of Sonication Followed by 5 Minute LMX4 Application Compared With 30 Minute LMX4 Application for Topical Anesthesia Prior to Subcutaneous Port Access in Children
Status: COMPLETED
Status Verified Date: 2012-02
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: Children ages 3-17 who are undergoing port access receive both standard care topical medicine for numbing LMX4 and the study intervention which utilizes ultrasound to speed the onset of LMX4 from 30 minutes to 5 minutes The procedures will be performed on 2 separate visits to the clinic The childs pain with the access procedure is evaluated
Detailed Description: None

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