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Electroencephalographic mechanism of dexmedetomidine deepening sevoflurane anesthesia in young children

Electroencephalographic mechanism of dexmedetomidine deepening sevoflurane anesthesia in young children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080377
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

general anesthesia

Interventions

Dex group (experimental):Dexmedetomidine was pumped after induction and maintenance of general anesthesia with sevoflurane
Saline group (control):Normal saline was pumped after induction and maintenance of general anesthesia with sevoflurane

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1: Plan to undergo selective non-craniocerebral and non-cardiac pediatric surgery under general anesthesia 2: Aged 2-12 years 3: Full-term delivery 4: Procedures were 2 hours or longer 5: ASA score is ?~?

Exclusion criteria

Exclusion criteria: 1: There were growth retardation, cerebrovascular accident, mental illness, severe cognitive impairment, epilepsy and other nervous system Systematic adverse events 2: Parents with conditions that hinder communication and preoperative evaluation, such as severe hearing or vision impairment 3: Previous history of general anesthesia surgery 4: Patients with head trauma/infection, severe eczema, skin allergy or allergy are not suitable for EEG monitoring 5: Preoperative infusion of sedatives (less than 24 hours), including propofol, morphine, fentanyl, midazolam, chloramine Ketone and dexmedetomidine 6: Patients who are known to be allergic to the active ingredient of dexmedetomidine, or have contraindications to the use of dexmedetomidine such as heart disease Bradykinesia, hypotension or severe cardiac dysfunction 7: Emergency surgery or parents refused to participate in the study

Design outcomes

Primary

MeasureTime frame
Electroencephalogram parameters;

Secondary

MeasureTime frame
Richmond Agitation-Sedation Scale, RASS;Pain-Numerical rating scale;The Post-Hospitalisation Behaviour Questionnaire, PHBQ;The Strengths and Difficulties Questionnaire, SDQ;postoperative complications;

Countries

China

Contacts

Public ContactMeiying Cui

Shengjing Hospital of China Medical University

cmynana@163.com+86 189 4025 4482

Outcome results

None listed

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