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Half effective dose of oral dexmedetomidine for sedation in children undergoing non-cardiac surgery

Half effective dose of oral dexmedetomidine for sedation in children undergoing non-cardiac surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039398
Enrollment
Unknown
Registered
2020-10-25
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-02-01

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

Conditions

Anxiety

Interventions

Oral Dexmetomidine Group:The oral dose of Dexmetomidine was adjusted up and down according to the Ramssay score when the child was separated from his parents.

Sponsors

The First Affiliated Hospital of USTC, Southern District (Anhui Provincial Hospital, Southern District)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1.Preschool children aged 3-6 years old undergoing elective non-cardiac surgery; 2.ASA I-II grade; 3.The family member signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Preoperative mYPAS 2 hours; 3. Important organs surgery; 4. Congenital heart disease; nervous system disease; upper respiratory tract infection, bronchial asthma; severe obesity; liver and renal function disfuction; 5. Allergy to Dexmetomidine.

Design outcomes

Primary

MeasureTime frame
Ramsay sedation score;—

Countries

China

Contacts

Public ContactJia Yang

The First Affiliated Hospital of USTC, Southern District (Anhui Provincial Hospital)

yangjiahao79@163.com+86 13965059649

Outcome results

None listed

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