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Combined Spinal-Epidural Temperature and Duration of Action

Pain Clinical Trial

Official title:
Effect of Temperature of Combined Spinal Epidural Dosing on Duration

Clinical Trial Summary

The hypothesis is that a combined spinal-epidural drug at refrigerated temperature will have a shorter period of pain relief than that maintained at room temperature. The temperature of the dose of medication will be measure with an infrared thermometer immediately prior (within 5 minutes) to administration.

Clinical Trial Description

Subjects will receive a combined spinal epidural medication as per standard of care to treat their labor pain; however, they will be randomized to receive either a dose maintained at room temperature (60-75 degrees F) or one maintained in a refrigerator (~<43 degrees F). Duration of action will be done by assessments of pain, vital signs, nausea, itching, bromage and fetal heart rate every 15 minutes until the subject requests additional pain medication to treat their labor pain. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02020304
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Completed
Phase Phase 2
Start date August 29, 2013
Completion date May 4, 2014
View Details
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