Clinical Trials Directory

Trials / Completed

CompletedNCT02907957

Infrared Thermography for Assessment of Caudal Block in Children

A Clinical Evaluation Of Infrared Thermography To Assess Successful Caudal Block In Children

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago · Academic / Other
Sex
All
Age
6 Months – 5 Years
Healthy volunteers
Accepted

Summary

Regional analgesia via caudal neuraxial blockade provides pain relief for pediatric patients following urological and lower extremity procedures. The injection of local anesthetic into the caudal epidural space causes a sensory loss. This sympathetic blockade in turn causes a vasodilation, or increased blood flow, to the lower extremities. The purpose of this study is to determine whether the FLIR ONE thermographic camera, a smartphone attachment which utilizes an application ("app") to measure the temperature at a site on an image of the lower extremity, will be able to differentiate between caudal, non-caudal, and failed caudal images.

Conditions

Interventions

TypeNameDescription
DEVICEFLIR ONEThermographic assessment of the lower extremities is obtained using the FLIR ONE smartphone camera and software.
PROCEDURERegional Anesthesia - Caudal Nerve BlockNerve block placement as a pain management strategy indicated for certain urological and lower extremity surgeries.

Timeline

Start date
2016-09-01
Primary completion
2018-06-01
Completion
2018-06-28
First posted
2016-09-20
Last updated
2019-08-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02907957. Inclusion in this directory is not an endorsement.