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OpenTrials
Completed

NCT Number: NCT01019746

Controlled Propofol Administration

The purpose of this study is to compare the administration of the standard anesthetic agent (propofol) using this automatic system with the manual administration of propofol by the anesthesiologist.

Completed

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Key information

Conditions

Hypnosis

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

MUHC - Montreal General Hospital

Montreal, Quebec, H3G 1A4, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients aged 18 to 90 years
  • surgery lasting more than 30 min

Exclusion criteria

  • inability to provide informed consent
  • allergies to study drug

Treatment and study plan

Propofol

Drug

propofol administration

Primary outcomes

  1. Comparison of control administration of propofol with manual administration.

    Time frame: 1 year

Secondary outcomes

  1. Emergence from anesthesia

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

McGill University Health Centre/Research Institute of the McGill University Health Centre

Other

Registry information

Official study title

Comparison of Closed-oop of Propofol Versus Manual Control Using Bispectral Index (BIS)

Important dates

Study start
2007
Primary completion
2008
First posted
Nov 25, 2009
Registry last updated
Nov 25, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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