Status:
COMPLETED
Breath Monitoring of Propofol (Observational Study)
Lead Sponsor:
Ludwig-Maximilians - University of Munich
Conditions:
Anesthesia
Eligibility:
All Genders
18+ years
Brief Summary
This trial investigates the relationship between concentrations of the anesthetic drug propofol in exhaled breath and blood in patients undergoing general anesthesia for elective surgery. The main goa...
Detailed Description
Propofol is a hypnotic drug commonly used for induction and maintenance of general anesthesia. Propofol is adiministered intravenously and has a comfortable side effect profile. Patients recover fast ...
Eligibility Criteria
Inclusion
- scheduled for routine surgery
- age ≥ 18 years
- planned duration of intervention \> 1 hour
- written informed consent
Exclusion
- propofol administration within 3 days prior to planned intervention
- pregnancy
- inability to give informed consent
- retraction of informed consent
Key Trial Info
Start Date :
May 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 1 2013
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT01892683
Start Date
May 1 2013
End Date
August 1 2013
Last Update
November 13 2013
Active Locations (1)
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1
Klinikum der Universität München, Campus Großhadern
München, Bavaria, Germany, 81377