Comparing Desflurane to Sevoflurane for the Effect on Recovery Time in Patients Undergoing Urolog… (NCT01219881) | Clinical Trial Compass
CompletedPhase 3
Comparing Desflurane to Sevoflurane for the Effect on Recovery Time in Patients Undergoing Urological Cystoscope Surgery
United States75 participantsStarted 2010-09
Plain-language summary
This is a single-center, prospective, randomized, double-blind, double-arm trial including 68 subjects scheduled to undergo urological cystoscope surgeries under general anesthesia (GA) with intubation through a laryngeal mask airway (LMA) at The Ohio State University Medical Center (OSUMC). Double blinding will be based on both the subject and the research staff being unaware of which trial arm the subject is randomized into. Eligible subjects that provide voluntary and written informed consent will be included in this study.
Who can participate
Age range50 Years – 75 Years
SexALL
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Inclusion criteria
✓. Male or female, 50 to 75 years of age.
✓. Subjects with an American Society of Anesthesiologist (ASA) physical status of I to III.
✓. Subjects able to provide written informed consent to participate in the study.
✓. Female subjects who have a negative urine or serum pregnancy test, who have been surgically sterilized, or are postmenopausal.
✓. Subjects scheduled for urological cystoscopic surgery under general anesthesia with LMA intubation.
Exclusion criteria
✕. Subjects who are prisoners.
✕. Subjects who have limited decision-making capacity or lack the ability to consent.
✕. Subjects with a history of alcohol or drug abuse within the last year.
✕. Subjects with a history of an allergic reaction, intolerance, or contraindications to any of the study medications.