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Anesthetic Optimization in Scoliosis Surgery — AIS  

Postoperative Pain Clinical Trial

Official title:
Evaluation of an Anesthetic Optimization Technique in Adolescent Idiopathic Scoliosis Surgery

Clinical Trial Summary

The standard anesthetic care plan for people having adolescent idiopathic scoliosis surgery will be accompanied by a pharmacokinetic simulation of the administered drugs to suggest opportunities to adjust drug doses to achieve tolerable pain control after surgery, avoid respiratory depression and allow patients to respond quickly either during intraoperative testing or at the conclusion of surgery.

Clinical Trial Description

As part of this study, anesthesiologists will be given additional data on the expected drug effects based on a computer simulation. The data will be provided as a suggestion and will be used together with all the other information normally used to keep the study subjects safely asleep during surgery. In addition, data will be collected from the medical history and on postoperative pain control and medication side effects for the first 24 hours. Specifically, study subjects will be asked to rate their pain on a 10-point scale after they wake up from surgery and once they arrive in the pediatric intensive care unit. Measures of the time from the end of surgery until the study subjects are awake and out of the operating room will also be collected. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02481570
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase N/A
Start date November 2015
Completion date August 15, 2017
View Details
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