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Clinical Trial Summary

The purpose of this study is to describe infrared thermographic imaging as a tool for the assessment of epidural block in obstetrics patients


Clinical Trial Description

Patients will recive standard anesthesia care for epidural placement and additionally, thermographic imaging will be obtained at baseline and up to 30 min after the epidural blockade is performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02739776
Study type Observational
Source Cook County Health
Contact
Status Withdrawn
Phase
Start date February 2, 2016
Completion date November 17, 2017

See also
  Status Clinical Trial Phase
Completed NCT04981158 - Enhanced Recovery After Lumber Laminectomy Using Epidural and General Anesthesia N/A