The precision of three pain scales as a function of sedatio
- Conditions
- This is a patient study in patients with a planned operation under general anaesthesie including healthy or merately ill patients (anaesthesia risk classification ASA 1-3).Pain self assessment as a function of sedation by IMP is studied.
- Registration Number
- EUCTR2008-003586-45-AT
- Lead Sponsor
- Department of Anaesthesie, General Intensive Care and Pain Therapy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- All
- Target Recruitment
- Not specified
Painless patients with a planned operation and anaesthesie
Consent into generally anaesthesia
Consent into the study
Completed 18 year of life
ASA-Classification 1-3
Availability of a seeing aid in case of a amblyopia
Hearing aid in case of a hypakusis
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
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
Patients with no planned operation
Contraindications against general anaesthesia
Confessed allergy against propofol
Patients under 18 years
Pregnant women
ASA-Classification 4
heavy respiratory disease
anxiety disorder or other psychological disorder
intake of analgetics 24 hours before studie starts
amblyopia
intake of anxiolytika before operation
hypakusis
insufficient knowledge of german language
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method