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The influence of volatile induction and maintenance anesthesia with sevoflurane and desflurane on postoperative agitation, delirium and cognitive disorder in pediatric anesthesia

The influence of volatile induction and maintenance anesthesia with sevoflurane and desflurane on postoperative agitation, delirium and cognitive disorder in pediatric anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011915
Enrollment
Unknown
Registered
2017-07-09
Start date
2017-11-01
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

paediatric postoperative cognitive disorder

Interventions

S group:volatile induction and maintenance anesthesia(VIMA) with sevoflurane
SD group:desflurane anesthesia after sevoflurane inhaled induction
SP group:propofol intravenous maintenance after sevoflurane inhaled induction
P group:total intravenous anesthesia?(TIVA) with propofol
PD group:desflurane inhaled maintenance after propofol induction

Sponsors

The First Affiliated Hospital, University of South China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. children aged 5-12 years; 2. scheduled to undergo elective adenotossillectomy and/or Adenoidectomy; 3. children with American Society of Anesthesiologists (ASA) physical status I or II; 4. intelligence quotient(IQ) = 90 under preoperative Peabody Picture Vocabulary Test(PPVT); 5. signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. children with developmental delay, mental retardation, dysgnosia and language disorders; 2. children with neurological disorders or psychiatric illness before the surgery; 3. children with cardiovascular, respiratory, hapatic, renal, endocrine,or immuce diseases; 4. children with abnormal airway, asthma or other reactive airway disease; 5. children with history of general anesthesia or long time exposure to general anesthesia before the surgery; 6.children without any premedication(e.g. anticholinergic agents or sedative-hypnotic drugs, etc.); 7.communication or follow-up problems with inspector of children.

Design outcomes

Primary

MeasureTime frame
the incidence of emergence agitation;the 5-point scale score ;pediatric anesthesia emergence delirium( PAED)scale;Children's and Infants' Postoperative Pain Scale (CHIPPS);Face, Legs, Activity, Cry, Consolability (FLACC) scale;Peabody Picture Vocabulary Test (PPVT);Combined Raven's Test (CRT);Wechsler intelligence scale for children ;S100ß;neuron-specific enolase (NSE) ;

Countries

China

Contacts

Public ContactLiu Wenjie

The First Affiliated Hospital, University of South China

149144040@qq.com+86 13037344744

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026