EUCTR2006-003720-11-BE
Active, not recruiting
Not Applicable
Comparison of the quality of anesthesia and intraoperative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia using endocrinologic and immunologic markers and an off-line, post-hoc calculated surgical stress index during anesthesia with different steady-state concentrations of remifentanil and spectral entropy guided propofol administration
GE Healthcare Finland Oy0 sitesAugust 30, 2006
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- GE Healthcare Finland Oy
- Status
- Active, not recruiting
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ASA I and II
- •male or female patients
- •aged 18\-65 years
- •scheduled for surgery planned in the Operation Room schedule for more than 1 hour of duration.
- •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) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Weight less than 70% or more than 130% of ideal body weight
- •Neurological disorder
- •Thyroid disorder
- •Recent use of psycho\-active medication, including alcohol.
- •Patients taking any medication influencing heart rate variability (such as inotropic drugs, vagolytic drugs, beta\-blockers, etc…).
- •Patients having allergy to the study medication.
- •Patients with a positive pregnancy test.
- •Patients being included in another trial within 30 days prior to this study screening
Outcomes
Primary Outcomes
Not specified
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