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Clinical Trials/EUCTR2008-008193-31-FR
EUCTR2008-008193-31-FR
Active, not recruiting
Not Applicable

Impact des facteurs chronologiques et démographiques sur les posologies per-opératoires des agents anesthésiques (Etude prospective multicentrique) - PosoAnes

Hopital Foch0 sites4,500 target enrollmentFebruary 6, 2009
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Conditionsgeneral anesthesiaMedDRA version: 9.1Level: LLTClassification code 10002323Term: Anesthesia general
DrugsUltivaPropofol

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
general anesthesia
Sponsor
Hopital Foch
Enrollment
4500
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 6, 2009
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Patients scheduled for general anesthesia
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\- age lower than 18 years,
  • •\- pregnancy, nursing women
  • •\- combination of general anesthesia and loco\-regional anesthesia,
  • •\- allergy to latex, propofol, remifentanil, morphine, muscle relaxant, or to a component,
  • •\- patients receiving a psychotropic treatment, and patients taking agonist\-antagonist opiates,
  • •\- presence of a central neurological disorder or a lesion cerebral,
  • •\- history of hypersensibility to remifentanil or to a derivate of fentanyl,
  • •\- presence of a pace\-maker,
  • •\- surgery on the skull or operating position preventing the use of bispectral index sensor in suitable conditions.

Outcomes

Primary Outcomes

Not specified

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