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COMPLETEDNANCT01202162

A Comparison of Desflurane vs. Sevoflurane and the Time to Awakening and the Incidence and Severity of Cough

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...

Lead sponsor: Northwestern University•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Northwestern University

Age

18 - 65 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Age 18-65
•Female patients undergoing outpatient gynecologic and breast surgery
•Under general anesthesia using an LMA
•ASA I,II,

Exclusion Criteria

•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

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: November 25, 2013Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment85

Start dateFeb 2010

Last updatedNov 25, 2013

Condition

Surgery Anesthesia

Locations shown

Northwestern University

Chicago, Illinois

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 25, 2013Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions