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Clinical Trials/NCT01411020
NCT01411020
Completed
Phase 4

Target-controlled Infusion (TCI) of Propofol for Induction in Children 3 to 11 Years

Pontificia Universidad Catolica de Chile1 site in 1 country60 target enrollmentOctober 2009

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Children Under General Anesthesia
Sponsor
Pontificia Universidad Catolica de Chile
Enrollment
60
Locations
1
Primary Endpoint
dose of propofol
Status
Completed
Last Updated
12 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
November 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ricardo Fuentes Henriquez

Profesor Asistente, Departamento de Anestesiología

Pontificia Universidad Catolica de Chile

Eligibility Criteria

Inclusion Criteria

  • obtained informed consent
  • children between 3 and 11 years
  • 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

Outcomes

Primary Outcomes

dose of propofol

Time Frame: two days (duration of hospitalization)

to obtain a dose appropriate of propofol in induction of anesthesia

Study Sites (1)

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