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

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age19+
SponsorChung-Ang University Gwangmyeong Hospital

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Patients who refused to participate in the study

Pregnant patients

Patients with a history of hypersensitivity to drugs or additives used during surgery

Patients with acute narrow-angle glaucoma

Trial design

Treatments tested in this trial

  • Remimazolam
  • Propofol

Treatment groups

116 Participants
are divided into 2 treatment groups