Status:
COMPLETED
Monitoring Exhaled Propofol to Individualize General Anesthesia
Lead Sponsor:
University of California, San Francisco
Conditions:
General Anesthesia
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This trial investigates the relationship between concentrations of the anesthetic drug propofol in exhaled breath, blood and drug effect in volunteers undergoing general anesthesia. The main goal of t...
Eligibility Criteria
Inclusion
- 18 years of age
- Written informed consent
- Ability and willingness to give written informed consent
- American Society of Anesthesiologists (ASA) risk score I
Exclusion
- Volunteers ASA physical status II - III
- Pregnancy
- Volunteers with history of neurological disease or stroke
- Volunteers with a history of recreational drug abuse
- Volunteers with a history of alcohol abuse
- Smokers
- Anesthesia within 6 months
- Known drug allergies
- History of adverse events during general anesthesia
Key Trial Info
Start Date :
August 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2010
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT01191021
Start Date
August 1 2010
End Date
October 1 2010
Last Update
June 5 2013
Active Locations (1)
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1
Department of Anesthesia and Perioperative Care, UCSF
San Francisco, California, United States, 94122