A Comparison of Novel with Conventional Propofol Dosing Regimen for Procedural Sedation in Pediatric Patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002428

Enrollment

180

Registered

2017-08-25

Start date

2017-08-23

Completion date

Unknown

Last updated

2022-03-08

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

Conditions

None listed

Interventions

Drug : Patients were randomly assigned to the experimental group and the control group according to the randomization table administered by the researcher, using the 'sample' function of the statistic

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Selection criteria; Patients who were referred to the pediatric sedation for diagnostic imaging (CT, MRI) I. ASA(American Society of Anesthesiology physical status) class I~II Ii. Pediatric patients aged 1 to 12 years Iii. Patients requiring sedation for MRI or CT scans scheduled for less than 20 minutes Iv. Pediatric patients with parental consent

Exclusion criteria

Exclusion criteria: Exclusion criteria; If any of the following items are met, they are excluded. I. ASA(American Society of Anesthesiology physical status) class III, IV Ii. Cardiopulmonary disease Iii. Upper respiratory tract infection Iv. Anatomical deformity of the airway V. Tonsillar hypertrophy Vi. Propofol sensitization Vii. Fat metabolism disorder

Design outcomes

Primary

Measure	Time frame
Complication occurrence	—

Countries

Korea, Republic of

Contacts

Public Contacthyojin byon

Yonsei University

jinoben@naver.com+82-2-2228-2429

Outcome results