Clinical Trials Directory

Trials / Completed

CompletedNCT02489734

Post Extubation Delirium and End-tidal Sevoflurane Concentration

Association Between Post Extubation Delirium and Pre-extubation End-tidal Sevoflurane Concentration in Children

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
109 (actual)
Sponsor
Children's Hospital of Fudan University · Academic / Other
Sex
All
Age
2 Years – 7 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the incidence of emergence delirium will be reduced when end-tidal concentration of sevoflurane decreases.

Detailed description

Sevoflurane induction and maintenance were selected. Intubation was performed after lidocaine spray on vocal cord. After that, an effective caudal or brachial plexus block was performed. End-tidal concentration of sevoflurane was maintained at 2.5%. Spontaneous respiratory was maintained. Sevoflurane was stopped after the end of surgery. Patients were randomly assigned to 2 groups: high concentration group (Group HC, end-tidal concentration of sevoflurane when extubating \>=0.5%) and low concentration group (Group LC, end-tidal concentration of sevoflurane when extubating \<0.5%). Patients in Group LC were extubated when they coughed or purposeful movement appeared. The patients whose end-tidal concentration of sevoflurane \>= 0.5% were excluded. Patients in Group HC were extubated when any of the criteria was met: 1.the patient coughed or purposeful movement appeared 2.end-tidal concentration of sevoflurane decreased to 0.5%. A trained nurse (blind to groups) recorded PAEDs scores in PACU.

Conditions

Interventions

TypeNameDescription
DRUGsevofluraneextubation when end-tidal concentration of sevoflurane \< 0.5%
DRUGSevofluraneextubation when end-tidal concentration of sevoflurane \>= 0.5%

Timeline

Start date
2015-07-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2015-07-03
Last updated
2021-08-19
Results posted
2021-08-19

Source: ClinicalTrials.gov record NCT02489734. Inclusion in this directory is not an endorsement.