Changes of Dorsalis Pedis Artery Flow Pattern After Caudal NCT01107873

Updated 06/14/2024

Clinical Trial Details — Status: Completed

Administrative data
NCT number	NCT01107873
Other study ID #	4-2010-0085
Secondary ID
Status	Completed
Phase	N/A
First received	April 19, 2010
Last updated	October 6, 2010
Start date	May 2010
Est. completion date	June 2010

Study information
Verified date	October 2010
Source	Yonsei University
Contact	n/a
Is FDA regulated	No
Health authority	Korea: Food and Drug AdministrationKorea: Ministry for Health and Welfare
Study type	Observational

Clinical Trial Summary

The purpose of this study is to determine the changes of Dorsalis Pedis Artery Flow Pattern after Caudal Block in Children: Observational Study Using a Duplex Sonography.

Recruitment information / eligibility
Status	Completed
Enrollment	20
Est. completion date	June 2010
Est. primary completion date	June 2010
Accepts healthy volunteers	No
Gender	Male
Age group	1 Year to 5 Years
Eligibility	Inclusion Criteria: - Twenty (ASA status I) unpremedicated children, ages 1 to 5 yr old, who were scheduled for a day-case urologic surgery Exclusion Criteria: - if there were contraindications for caudal block including hypersensitivity to any local anaesthetics, bleeding diathesis, infections at the puncture sites, or pre-existing neurological disease.

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Anesthesia, Caudal

Locations
Country	Name	City	State
n/a

Sponsors *(1)*
Lead Sponsor	Collaborator
Yonsei University

Outcome
Type	Measure	Description	Time frame	Safety issue
Primary	Investigation of arterial hemodynamics	Investigation of arterial hemodynamics included peak systolic velocity [PS], end diastolic velocity [ED], mean velocity [MV], time-averaged maximum velocity [TAmax], time-averaged mean velocity [TAmean], pulsatility index [PI], volume flow [VF], and dorsalis pedis artery diameter [D].		No

See also
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