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Comparison of Desflurane With Sevoflurane for School-age Children in Postoperative Cognitive Function

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02909413
Enrollment
600
Registered
2016-09-21
Start date
2016-10-31
Completion date
2020-10-31
Last updated
2016-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Cognitive Dysfunction

Keywords

desflurane, sevoflurane

Brief summary

This study compares desflurane with sevoflurane for school-age children in postoperative cognitive function.

Detailed description

The postoperative cognitive dysfunction (POCD) of school-age children (6-14 age) after operation draw more attention from both society and family. It is well known that, compare with sevoflurane, desflurane could improve cognitive function in elderly patients. But whether Desflurane could improve postoperative cognitive function compare with Sevoflurane for the school-age children, there is no consistent conclusion.

Interventions

Anesthesia maintenance: After endotracheal intubation, half of the patients will be randomized into Desflurane Group. The gas flow rate of Desflurane group is 2 L/min, include 50% O2 and 4~5% Desflurane.

DRUGsevoflurane

Anesthesia maintenance: After endotracheal intubation, half of the patients will be randomized into Sevoflurane Group. The gas flow rate of Desflurane group is 2 L/min, 50%O2 and 1.7-2.0% Sevoflurane.

Sponsors

Shengjing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* 6-14 age, elective no-cardiac and non-neurological surgery , ASA physical statusⅠorⅡ, no preoperative cognitive function impairment, cooperate to complete the entire test.

Exclusion criteria

* Allergic to halogens inhaled anesthetics, malignant hyperthermia susceptible patients, intracranial hypertension, emotional disorder, hyperactivity, history of operation, mental retardation, audio-visual obstacles, history of congenital heart disease, Important organ dysfunction, history of drug abuse * History of epilepsy * Preoperative respiratory infection significantly.

Design outcomes

Primary

MeasureTime frameDescription
The incidence of postoperative cognitive dysfunctionWithin 7 days after operationCognitive function score should be carried out for all children at preoperative 1d, postoperative 2 d, 3d and 7d. If postoperative score compared with preoperative score drop 1 points or more, then postoperative cognitive dysfunction will be recorded.

Secondary

MeasureTime frameDescription
male1 day before operationIf the child is boy,it's yes,or it's no.
height1 day before operationCM
weightpreoperationkg
previous operation historypreoperationIf the child had previous operation history,it's yes,or it's no.
the duration of anesthesiaFrom the time began to give the anesthetic to the time of pull out the endotracheal intubationminutes
the duration of operationSurgery end time minus the start timeminutes
age1 day before operationyears old
total volume of infusionThe total volume of infusion of the whole surgery time.ml
whether there is respiratory depression in postanesthesia care unitThe period which the patient stay at post anesthesia care unit,from the time enter to postanesthesia care unit to the time leave postanesthesia care unit,the estimated period is up to 30 minutes.If the child has respiratory depression during this time,it's yes,or it's no.
the length of hospital staythe time from admission to hospital to discharge from hospital,the estimated period is up to 5 days.days
S100β1 day after surgeryobtain the children's plasma to detection S100β with ELEASE.
NSE1 day after surgeryobtain the children's plasma to detection NSE with ELEASE.
total blood lossThe total blood loss of the whole surgery time.ml

Contacts

Primary ContactYingjie Du, MD
duyingjiemazui@163.com+86-18940252852

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026