TerminatedPhase 3ketamine

Ketamine and Closed-Loop Anesthesia System

Sponsored by Hopital Foch

NCT ID
NCT02011347
Target Enrollment
67 participants
Start Date
2013-07
Est. Completion
2015-10-07

About This Study

The objective is to evaluate the sparing effect of ketamine on the dose of propofol.

Conditions Studied

Anesthesia

Interventions

  • Ketamine
  • Placebo

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* patients with an American Society of Anesthesiology score 1, 2 or 3
* scheduled for a surgical procedure lasting more than 2 hours under general anesthesia

Exclusion Criteria:

* pregnancy
* chronic pain
* simultaneous general and loco-regional anesthesia
* contra-indication to to nonsteroidal anti-inflammatory drug
* contra-indication to Ketamine
* contra-indication to propofol, to remifentanil, to morphine
* history of central nervous system disease
* patients receiving a psychotropic treatment
* patients with a pace-maker

Study Locations (2)

Hopital Foch
Suresnes, Hauts de Seine, France
Clinique Fontaine les Dijons
Fontaine-lès-Dijon, France

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source