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The effect of dexmedetomidine on emergence agitation in children receiving sevoflurane-based anethesia

The effect of dexmedetomidine on emergence agitation in children receiving sevoflurane-based anethesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCH-12002511
Enrollment
Unknown
Registered
2012-08-19
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

emergence agitation in children receiving sevoflurane-based anesthesia

Interventions

saline group:propofol 1mg/kg
1:dexmedetomidine

Sponsors

Department of Anesthesiology, Second Affiliated Hospital of Harbin Medical University, Heilongjiang Key Laboratory of Anesthesiology andIntensive Care Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 8 Years

Inclusion criteria

Inclusion criteria: ninety children,aged 2-8 years,ASA I-II,weighted 10-40kg,receiving sevoflurane undergoing adenotossillectomy and/or Adenoidectomy.

Exclusion criteria

Exclusion criteria: a history of psychiatric disease;cardiovascular ,respiratory,hapatic,renal,endocrine,or immuce diseases

Design outcomes

Primary

MeasureTime frame
5-point scale to evaluate emergence agitatio;—

Countries

China

Contacts

Public ContactXi Hongjie
xihongjie1973@hotmail.com+86 13796652407

Outcome results

None listed

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