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Recruiting Observational

Anesthesia Neurodevelopmental Impact in Congenital Scoliosis Children

NCT06315933 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2020-07-13
Last updated
2025-11-18

Condition(s) studied

General Anesthetics Toxicity

Investigational drug(s) / intervention(s)

General anesthesia

General anesthesia: General anesthesia including inhaled and intravenous

Study summary

In the past, a large number of animal studies have suggested that anesthesia exposure has potential neurotoxic effects, resulting in persistent cognitive and behavioral deficits. At present, there is still a lack of sufficient clinical research evidence to prove whether anesthesia exposure has long-term effects on neurodevelopment. The existing clinical research data suggests that a single short-time anesthesia exposure in young children does not affect long-term neurodevelopmental outcomes. Early onset scoliosis, including congenital scoliosis, is a type of scoliosis deformity that occurs before the age of 10. Posterior scoliosis correction surgery is one of the common treatment. There is currently no research indicating the impact of early single or multiple long-duration anesthesia exposure on the neurological development of children with congenital scoliosis. The aim of this study is to determine the long-term effect of general anesthesia exposure on neurocognitive function and behavior in children with congenital scoliosis, in order to provide reference for related clinical work.

Eligibility

Sex
ALL
Min age
6 Years
Max age
16 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with congenital scoliosis * 6-16 years old at the time of assessment Exclusion Criteria: * Cognitive impairment caused by congenital, traumatic or other reasons; * Existence of mental or psychological disorders; * There are factors that may affect neurological development, including any known central nervous system disease, neurological injury, or history of neonatal asphyxia; * Unable to cooperate with cognitive function tests; * The child is unable to communicate in Chinese.

Primary outcome measure(s)

  • full-scale intelligence quotient, FSIQ — At the time of collecting baseline demographic data
    Measured by Wechsler Intelligence Scale for Children-Fourth Edition (WISC-IV)

Trial sites (1)

FacilityCityRegionStatus
Peking Union Medical College Hospital Beijing Beijing Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06315933 on ClinicalTrials.gov ↗ ← All trials in China