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

Not Applicable

Completed

• Conditions: Not Applicable

• Registration Number: KCT0002428
• Lead Sponsor: Yonsei University Health System, Severance Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-10-12
• Last Update Posted: 8 March 2022

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 180

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; 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

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Complication occurrence