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

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002429

Enrollment

Registered

2017-08-25

Start date

2017-06-01

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Drug : If the patient&#39

s participation in the study is determined before the inspection time, check the participation in the study once before entering the laboratory. Then, when the patient enters the laboratory, the blood

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) selection criteria; Patients who were admitted to the hospital or who were present at the hospital and who were referred to the pediatric complaint for diagnostic imaging (CT, MRI) I. ASA(American Society of Anesthesiologists) 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

Exclusion criteria

Exclusion criteria: Exclusion criteria; Excluded if any of the following items are met: I. ASA(American Society of Anesthesiologists) class III, IV Ii. Cardiopulmonary disease Iii. Anatomical deformity of the airway Iv. Tonsillar atrophy V. Fat metabolism disorder

Design outcomes

Primary

Measure	Time frame
Incidence of side effects	—

Secondary

Measure	Time frame
Recovery time from sedation	—

Countries

Korea, Republic of

Contacts

Public Contacthyojin byon

Yonsei University

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

Outcome results