Dexmedetomidine combined with propofol intravenous sedation in outpatient imaging in children: a randomized controlled clinical study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000033541

Enrollment

Unknown

Registered

2020-06-04

Start date

2020-07-01

Completion date

Unknown

Last updated

2020-06-08

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

Conditions

Outpatient sedation in children

Interventions

Group Propofol:Propofol iv sedation

Group Chloral hydrate:Oral take 10% chloral hydrate by 0.5ml/kg sedation

Group Dex & Pro:Dex&Pro iv sedation

Eligibility

Sex/Gender

All

Age

No minimum to 6 Years

Inclusion criteria

Inclusion criteria: Children aged 0~6 years with ASA I~ III who underwent imaging examination in outpatient department.

Exclusion criteria

Exclusion criteria: Nil

Design outcomes

Primary

Measure	Time frame
Sedation onset time;Time from drug administration until wake up;Time to wake up after completion of the procedure;	—

Secondary

Measure	Time frame
complications;Vital signs;satisfaction score;	—

Countries

China

Contacts

Public ContactChen Jinghui

Guangzhou Women and Children Medical Center

13570300715@163.com+86 13570300715

Outcome results

None listed

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