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Anesthetic Optimization in Scoliosis Surgery

NCT02481570 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2019-08-12

No results posted yet for this study

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.

Conditions

  • Adolescent Idiopathic Scoliosis
  • Respiratory Depression
  • Postoperative Pain

Interventions

OTHER

pharmacokinetic simulation

The aim of the simulation is to recommend dosing adjustments to improve postoperative analgesia with a rapid emergence.

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Christoph Seubert, MD PhD DABNM · University of Florida

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2016-11-21
Completion
2017-08-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02481570 on ClinicalTrials.gov