Skip to content

Clinical Study of Intranasal Dexmedetomidine Combined with Situational Preview Audio-Visual Intervention on Postoperative Delirium in Preschool Children Undergoing Ophthalmic General Anesthesia

Clinical Study of Intranasal Dexmedetomidine Combined with Situational Preview Audio-Visual Intervention on Postoperative Delirium in Preschool Children Undergoing Ophthalmic General Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121133
Enrollment
Unknown
Registered
2026-03-26
Start date
2026-03-26
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Emergence delirium

Interventions

Group B (dexmedetomidine):dexmedetomidine
Group C (Scenario Preview Listening):Scenario Preview Audio
Group A (Dexmethomidine + Scenario Preview Listening):Dexmedetomidine + Scenario preview listening
Group D (Control Group):Control group

Sponsors

Ningbo Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1. Having clear surgical indications and complete clinical medical records; 2.Preschool children aged 3 to 6 years old, regardless of gender; 3.Body Mass Index (BMI) less than 23; 4.American Society of Anesthesiologists (ASA) physical status classification ? to ?.

Exclusion criteria

Exclusion criteria: 1.Patients with upper respiratory tract infection within 2 weeks before surgery; 2.Patients with sinus bradycardia or atrioventricular block; 3.Patients with mental abnormalities, intellectual disability, hearing impairment, or those who received other narcotic analgesic and sedative drugs within 24 hours; 4.Patients with severe abnormal cardiac, hepatic and renal functions; 5.Patients with operation duration longer than 2 hours; 6.Patients undergoing non-first-time surgery; 7.Patients whose family members refused to participate in the study.

Design outcomes

Secondary

MeasureTime frame
Choking cough reaction during extubation;Safety Evaluation;FLACC pain score;Operation time, extubation time (from drug withdrawal to extubation), and PACU stay time;PAED scale score;

Countries

China

Contacts

Public ContactZhang Danfeng

Ningbo Eye Hospital

420612701@qq.com+86 159 5748 1357

Outcome results

None listed

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