Comparison of Remimazolam and Propofol for Recovery of Ambulatory Upper Airway Surgery

Recruiting Phase 4 Interventional Study
Laryngeal Disease Pharyngeal Diseases Oral Cavity Disease Nasal Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
19 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
116 (estimated)
Sponsor
Chung-Ang University Gwangmyeong Hospital · Other
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About This Trial

The purpose of this study is to compare the effects of remimazolam and propofol on postoperative recovery time, complications, and safety in patients undergoing ambulatory upper airway surgery under general anesthesia.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult patients (age 19 or older) undergoing ambulatory upper respiratory tract (nasal cavity, oral cavity, pharynx, larynx) surgery under general anesthesia * American Society of Anesthesiologists physical class classification I, II, and III Exclusion Criteria: * Patients wh…
Contacts

Se-Hee Min

+820222221534

seiheemin@gmail.com

CONTACT