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Clinical Trials/EUCTR2013-001592-20-NL
EUCTR2013-001592-20-NL
Active, not recruiting
Not Applicable

Pilot study for studying the influence of low-dose propofol on the classification of movements from the electroencephalogram in healthyparticipants

Not provided0 sitesJune 6, 2013
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ConditionsIntraoperative awareness during general anesthesiaTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsPropofol – Lipuro 10 mg/ml

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intraoperative awareness during general anesthesia
Sponsor
Not provided
Status
Active, not recruiting
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 6, 2013
End Date
TBD
Last Updated
12 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Not provided

Eligibility Criteria

Inclusion Criteria

  • •\-18\-65 years old
  • •\-right\-handed
  • •\-normal or corrected to normal vision
  • •\-normal or corrected to normal hearing
  • •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 12
  • •F.1\.3 Elderly (\>\=65 years) no
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\-neurological impairment
  • •\-motor disabilities
  • •\-known allergies or oversensitivity to propofol
  • •\-allergies to peanuts and/or soy
  • •\-cardiac respiratory, renal or hepatic impairment
  • •\-regular drug intake (of any kind, other than contraceptives and antihistamines)
  • •\-pregnancy or nursing

Outcomes

Primary Outcomes

Not specified

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