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The effectiveness of non-pharmacologic method for reducing postoperative emergence delirium in children: a prospective, randomized controlled study

The effectiveness of non-pharmacologic method for reducing postoperative emergence delirium in children: a prospective, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024846
Enrollment
Unknown
Registered
2019-07-30
Start date
2019-08-10
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Ophthalmic Diseases

Interventions

experimental group :non-pharmacologic method
control group:N/A

Sponsors

Shanghai Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 8 Years

Inclusion criteria

Inclusion criteria: 1. ASA score I or II; 2. ophthalmologic operation; 3. aged 3-8 years; 4. provide informed consent; 5. the first time undergo surgey;

Exclusion criteria

Exclusion criteria: 1.deaf or hearing impairment; 2.presence of developmental delays or neurological diseases; 3.hepatic and renal dysfunction.

Design outcomes

Primary

MeasureTime frame
the incidence of emergence delirium;—

Countries

China

Contacts

Public ContactYing Sun

Department of Anesthesiology, Shanghai Children's Medical Center

yingsun821@163.com+86 13621738118

Outcome results

None listed

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