Status:
COMPLETED
A Comparison of Desflurane vs. Sevoflurane and the Time to Awakening and the Incidence and Severity of Cough
Lead Sponsor:
Northwestern University
Conditions:
Surgery
Anesthesia
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Goals for ambulatory surgery include providing optimal surgical conditions while ensuring a rapid early recovery without side effect. Dexter et al1 concluded in a meta-analysis that Desflurane can red...
Eligibility Criteria
Inclusion
- Age 18-65
- Female patients undergoing outpatient gynecologic and breast surgery
- Under general anesthesia using an LMA
- ASA I,II,
Exclusion
- Patients on CNS depressants
- Chronic opioid use
- Corticosteroid
- Pregnant patients
- Full stomach
- Morbidly obese (BMI \>35kg/m2)
- Hepatitis B
- Hepatitis C
- Coronary artery disease
- Liver disease
- Renal disease
- Seizure disorder
- Dropout criteria:
- Need for endotracheal tube
- Surgeon or patient request
- Hospital admission
Key Trial Info
Start Date :
February 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2012
Estimated Enrollment :
85 Patients enrolled
Trial Details
Trial ID
NCT01202162
Start Date
February 1 2010
End Date
March 1 2012
Last Update
November 25 2013
Active Locations (1)
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1
Northwestern University
Chicago, Illinois, United States, 60611