Target-controlled Infusion of Propofol for Induction of Pediatric Anesthesia

Phase 4

Completed

• Conditions: Children Under General Anesthesia

• Registration Number: NCT01411020
• Lead Sponsor: Pontificia Universidad Catolica de Chile

Brief Summary

The purpose of this study is to determine a effect-site concentration of propofol in children 3 to 11 years effective to make a induction of general anesthesia.

Detailed Description

Not available

Study Timeline

• Status Verified: 2009-08
• Study Start: 2009-10
• Study First Submitted: 2011-08-03
• Study First Submitted QC: 2011-08-04
• Study First Posted: 2011-08-05
• Primary Completion: 2012-08
• Study Completion: 2012-11
• Last Update Submitted: 2013-05-14
• Last Update Posted: 2013-05-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• obtained informed consent
• children between 3 and 11 years
• healthy
• elective surgery under general anesthesia
• no premedication

Exclusion Criteria

• body mass index for age > 95th percentile
• chronic or acute intake of any sedative drug
• any known adverse effect to the study drugs

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
dose of propofol	two days (duration of hospitalization)	to obtain a dose appropriate of propofol in induction of anesthesia

Trial Locations

Locations (1)

Hospital Clinico Universidad Catolica; 🇨🇱 Santiago, Metropolitana, Chile